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HHS/FDA RIN: 0910-AH14 Publication ID: Spring 2016 
Title: General and Plastic Surgery Devices: Sunlamp Products 
Abstract:

This proposed rule would apply device restrictions to sunlamp products.

 
Agency: Department of Health and Human Services(HHS)  Priority: Economically Significant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Final Rule Stage 
Major: Yes  Unfunded Mandates: No 
EO 13771 Designation: uncollected 
CFR Citation: 21 CFR 878.4635   
Legal Authority: 21 U.S.C. 360j(e)   
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  12/22/2015  80 FR 79493   
NPRM Comment Period End  03/21/2016 
Final Action  11/00/2016 
Regulatory Flexibility Analysis Required: Yes  Government Levels Affected: State 
Small Entities Affected: Businesses  Federalism: Yes 
Included in the Regulatory Plan: No 
RIN Data Printed in the FR: Yes 
Related RINs: Related to 0910-AG30 
Agency Contact:
Ian Ostermiller
Regulatory Counsel, Center for Devices and Radiological Health
Department of Health and Human Services
Food and Drug Administration
10903 New Hampshire Avenue, WO 66, Room 5454,
Silver Spring, MD 20993
Phone:301 796-5678
Email: ian.ostermiller@fda.hhs.gov