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The Food and Drug Administration (FDA) is announcing the withdrawal of the proposed rule titled "General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use of Sunlamp Products," which published in the Federal Register of December 22, 2015. FDA is taking this action because it no longer intends to finalize the proposed rule.
Published
Mar 16, 2026
Citation
91 FR 12524
Agencies
2
Full text not available in our database.
View on Federal Register →Get a plain-English explanation of what this regulation does, which agencies are responsible, and how it affects existing rules.
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Docket No. FDA-2015-N-1765
0910-AH14
21 CFR 878