General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use of Sunlamp Products; Withdrawal of Proposed Rule
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.
Abstract as published in the Federal Register.
The complete document — every provision, the docket, and the comment instructions — is published in the Federal Register. SPEQ surfaces and indexes it for reference; the authoritative text lives on federalregister.gov.
View on federalregister.gov →Document details are published in the U.S. Federal Register; SPEQ surfaces them for reference and is not affiliated with or endorsed by the FDA or the Office of the Federal Register. The authoritative text is on federalregister.gov.