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HHS/FDA RIN: 0910-AH14 Publication ID: Fall 2015 
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: Other Significant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Proposed Rule Stage 
Major: Yes  Unfunded Mandates: No 
CFR Citation: 21 CFR 892.1750   
Legal Authority: 21 U.S.C. 360j(e)   
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  11/00/2015 
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:
Paul Gadiock
Regulatory Counsel
Department of Health and Human Services
Food and Drug Administration
Center for Devices and Radiological Health, 10903 New Hampshire Avenue, W0-66, Room 4432,
Silver Spring, MD 20993-0002
Phone:301 796-5736
Fax:301 847-8145
Email: paul.gadiock@fda.hhs.gov