[Federal Register Volume 82, Number 100 (Thursday, May 25, 2017)]
[Notices]
[Pages 24130-24131]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-10736]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2013-N-0879; FDA-2013-N-0579; FDA-2016-N-2474; FDA-
2016-D-1853; FDA-2013-N-0764; FDA-2013-N-0825; FDA-2013-N-0797; FDA-
2013-N-0578]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is publishing a list of
information collections that have been approved by the Office of
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations,
Food and Drug Administration, Three White Flint North, 11601 Landsdown
Street, North Bethesda, MD 20852, 301-796-7726, [email protected].
SUPPLEMENTARY INFORMATION: The following is a list of FDA information
collections recently approved by OMB under section 3507 of the
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control
number and expiration date of OMB approval for each information
collection are shown in table 1. Copies of the supporting statements
for the information collections are available on the Internet at
https://www.reginfo.gov/public/do/PRAMain. An Agency may not conduct or
sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB control number.
[[Page 24131]]
Table 1--List of Information Collections Approved by OMB
------------------------------------------------------------------------
OMB control Date approval
Title of collection No. expires
------------------------------------------------------------------------
Procedures for the Safe Processing and 0910-0354 2/29/2020
Importing of Fish and Fishery Products.
Biological Products: Reporting of 0910-0458 2/29/2020
Biological Product Deviations and Human
Cells, Tissues, and Cellular and Tissue-
Based Product Deviations; Form FDA 3486
and Addendum, 3486A....................
Designation of New Animal Drugs for 0910-0605 2/29/2020
Minor Use or Minor Species.............
Unique Device Identification System..... 0910-0720 2/29/2020
Animal Feed Regulatory Program Standards 0910-0760 2/29/2020
Premarket Approval of Medical Devices-- 0910-0231 3/31/2020
21 CFR Part 814........................
Human Tissue Intended for 0910-0302 3/31/2020
Transplantation........................
General Licensing Provisions: Biological 0910-0338 3/31/2020
License Application, Changes to an
Approved Application, Labeling,
Revocation and Suspension, and Form FDA
356h...................................
------------------------------------------------------------------------
Dated: May 18, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislative, and Analysis.
[FR Doc. 2017-10736 Filed 5-24-17; 8:45 am]
BILLING CODE 4164-01-P