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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. |
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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 |
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Timetable:
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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 |