Notices. Notice
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/register/2022/12/15/2022-27192·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4164-01-P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket Nos. FDA-2014-N-1048; FDA-2012-N-0386; FDA-2019-N-0430; FDA-2019-N-5553; FDA-2021-N-0555; FDA-2013-N-0242; and FDA-2019-N-1517] 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: JonnaLynn Capezzuto, Office of Operations, Food and Drug Administration, Three White Flint North, 10A-12M, 11601 Landsdown St., North Bethesda, MD 20852, 301-796-3794, *PRAStaff@fda.hhs.gov.* 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. Table 1—List of Information Collections Approved by OMB Title of collection OMB control No. Date approval expires Medical Devices; Humanitarian Use Devices 0910-0332 10/31/2025 Tobacco Product Establishment Registration and Submission of Certain Health Information 0910-0650 10/31/2025 Generic Clearance for Quick Turnaround Testing of Communication Effectiveness 0910-0876 10/31/2025 Right to Try Act: Reporting Requirements 0910-0893 10/31/2025 Medical Device Labeling Regulations 0910-0485 11/30/2025 Current Good Manufacturing Practices for Positron Emission Tomography
(PET)Drugs 0910-0667 11/30/2025 Abbreviated New Animal Drug Applications 0910-0669 11/30/2025 Dated: December 12, 2022. Lauren K. Roth, Associate Commissioner for Policy. [FR Doc. 2022-27192 Filed 12-14-22; 8:45 am]
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