[Federal Register Volume 63, Number 193 (Tuesday, October 6, 1998)] [Notices] [Pages 53677-53679] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 98-26647] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 98N-0364] Agency Information Collection Activities; Submission for OMB Review; Comment Request; Reporting and Recordkeeping for Electronic Products: Specific Product Requirements AGENCY: Food and Drug Administration, HHS. ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA) is announcing that the proposed collection of information listed below has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995 (the PRA). DATES: Submit written comments on the collection of information by November 5, 1998. ADDRESSES: Submit written comments on the collection of information to the Office of Information and Regulatory Affairs, OMB, New Executive Office Bldg., 725 17th St. NW., rm. 10235, Washington, DC 20503, Attn: Desk Officer for FDA. FOR FURTHER INFORMATION CONTACT: Margaret R. Schlosburg, Office of Information Resources Management (HFA-250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1223. SUPPLEMENTARY INFORMATION: In compliance with section 3507 of the PRA (44 U.S.C. 3507), FDA has submitted the following proposed collection of information to OMB for review and clearance. Reporting and Recordkeeping for Electronic Products: Specific Product Requirements (21 CFR Parts 1020, 1030, 1040, and 1050) (OMB Control Number 0910-0213)--Reinstatement Under sections 532 to 542 of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. 360ii to 360ss), FDA has the responsibility to protect the public from unnecessary exposure to [[Page 53678]] radiation from electronic products. Section 532 of the act directs the Secretary of the Department of Health and Human Services (the Secretary) to establish and carry out an electronic product radiation control program designed to protect the public health and safety from electronic radiation by, among other things, developing and administering performance standards for electronic products. Section 534(g) of the act directs the Secretary to review and evaluate industry testing programs on a continuing basis; and section 535(e) and (f) of the act directs the Secretary to immediately notify manufacturers of, and assure correction of, radiation defects or noncompliance with performance standards. The agency's authority to require records and reports is contained in section 537(b) and (c) of the act. Under this authority, FDA issued regulations detailing product- specific performance standards that specify information to be supplied with the product or require specific reports. The information collections are either specifically called for in the act or were developed to aid the agency in performing its obligations under the act. The data reported to FDA and the records that are maintained are used by FDA and the industry to make decisions and take actions that protect the public from radiation hazards presented by electronic products. This information refers to the identification of, location of, operational characteristics of, quality assurance programs for, and problem identification and correction of electronic products. The data provided to users and others are intended to encourage actions to reduce or eliminate radiation exposures. The consequence of not obtaining the required information is that the public unknowingly may be exposed to unnecessary radiation hazards presented by electronic products. Without this information, FDA could not adequately make rational decisions and take appropriate actions to protect the public from these hazards as called for in the act. Respondents to this collection of information are manufacturers, importers, and assemblers of electronic products. Not all of the requirements are placed on all of these groups. In the Federal Register of June 22, 1998 (63 FR 33933), the agency requested comments on the proposed collections of information. No significant comments were received. FDA estimates the burden of this collection of information as follows: Table 1.--Estimated Annual Reporting Burden1 ---------------------------------------------------------------------------------------------------------------- Annual 21 CFR Section No. of Frequency per Total Annual Hours per Total Hours Respondents Response Responses Response ---------------------------------------------------------------------------------------------------------------- 1020.20(c)(4) 1 1 1 1 1 1020.30(g) 200 1.33 265 35 9,275 1020.30(h)(1) through (h)(4) and 1020.32(a)(1) and (g)\2\ 200 1.33 265 35 9,275 1020.32(g) and 1020.33(c), (d), (g)(4), (j)(1), and (j)(2)\2\ 9 1.00 9 40 360 1020.40(c)(9)(i) and (c)(9)(ii) 8 1.00 8 40 320 1030.10(c)(4) 41 1.61 66 20 1,320 1030.10(c)(5)(i) through (c)(5)(iv)\2\ 41 1.61 66 20 1,320 1040.10(h)(1)(i) through (h)(1)(iv) 805 1.00 805 8 6,440 1040.10(h)(2)(i) and (h)(2)(ii)\2\ 100 1.00 100 8 800 1040.11(a)(2)\2\ 190 1.00 190 10 1,900 1040.20(d)(1), (d)(2), (e)(1), and (e)(2) 110 1.00 110 10 1,100 1040.30(c)(1) 1 1.00 1 1 1 1040.30(c)(2) 7 1 7 1 7 1050.10(f)(1) and (f)(2)(i) through (f)(2)(iii) 10 1.00 10 56 560 Disclosure Subtotal 1,176 1,186 32,679 1020.30(d)(1) and (d)(2) and Form FDA 2579 2,345 8.96 21,000 .30 6,300 1030.10(c)(6)(iii) 1 1.00 1 1 1 1030.10(c)(6)(iv) 1 1.00 1 1 1 1040.10(a)(3)(i) 83 1.00 83 3 249 1040.10(i)--burden in 1002.10 (0910-0025) 0 0 0 0 Reports Subtotal 2,430 21,085 6,551 Total Annual Reporting Burden 3,606 6.37 22,981 1.71 39,230 ---------------------------------------------------------------------------------------------------------------- \1\ There are no capital costs or operating and maintenance costs associated with this collection of information. \2\ The total number of respondents in the reporting burden, table 1, include respondents who have already been included as a subset of another group in the table. The number of firms marked by this superscript have been included and counted as a subset of the total firms subject to reporting burden. Therefore, the number of firms represented by this superscript have not been added to the total number of respondents on the entry for ``Disclosure Subtotal,'' and are not included in the total listed on the last entry of the reporting burden table entitled ``Total Annual Reporting Burden.'' However, any hours of burden generated by these firms were added to the total reporting burden hours on both the disclosure subtotal and total lines of the reporting burden table. Table 2.--Estimated Annual Recordkeeping Burden1 ---------------------------------------------------------------------------------------------------------------- Annual 21 CFR Section No. of Frequency per Total Annual Hours per Total Hours Recordkeepers Recordkeeping Records Recordkeeper ---------------------------------------------------------------------------------------------------------------- 1020.30(g)(2) 22 1 22 0.5 11 1040.10(a)(3)(ii) 83 1 83 1 83 Total Annual Recordkeeping Burden 94 ---------------------------------------------------------------------------------------------------------------- \1\ There are no capital costs or operating and maintenance costs associated with this collection of information. [[Page 53679]] Due to a typographical error, 21 CFR 1040.30(c)(2) was incorrectly placed in table 2 of FDA's previous notice seeking comment on this collection of information (63 FR 33933, June 22, 1998). The citation has been place in table 1 of this notice and the burden adjusted accordingly. Certain labeling requirements included in these regulations are either exempt from the definition of ``collection of information'' under 5 CFR 1320.3(c)(2) because they are ``public disclosure[s] of information originally supplied by the Federal Government to the recipient for the purpose of disclosure to the public'' or have negligible burden. For example, 21 CFR 1040.10(g) states that ``in addition to the requirements of Secs. 1010.2 and 1010.3, each laser product shall be subject to the applicable labeling requirements of this paragraph.'' The provision goes on to require several cautionary statements in the labeling of laser products approved under this regulation, and further specifies the wording, placement, and label design of the required labeling. Labeling requirements which are exempt from OMB are 21 CFR 1040.30(c)(1), 1050.10(d)(1) through (d)(5), and 1020.10(c)(4). The burden hour and cost estimates were derived by consultation with FDA and industry personnel. An evaluation of the type and scope of information requested was also used to derive some time estimates. For example, disclosure information primarily requires time only to update and maintain existing manuals. Initial development of manuals has been performed except for new firms entering the industry. When information is generally provided to users, assemblers, or dealers in the same manual, they have been grouped together in the ``Estimated Annual Reporting Burden'' table . Dated: September 28, 1998. William K. Hubbard, Associate Commissioner for Policy Coordination. [FR Doc. 98-26647 Filed 10-5-98; 8:45 am] BILLING CODE 4160-01-F