[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]


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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.

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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
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                                            OMB control    Date approval
           Title of collection                  No.           expires
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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...................................
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    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