Designation of Special Controls for Male Condoms Made of Natural Rubber Latex (21 CFR 884.5300); Small Entity Compliance Guide
On November 10, 2008, the Food and Drug Administration (FDA) published a final rule in the Federal Register, entitled “Obstetrical and Gynecological Devices; Designation of Special Controls for Male Condoms Made of Natural Rubber Latex” (73 FR 66522). This final rule amended the classification regulation for condoms under 21 CFR 884.5300 and designated a special controls guidance document for male condoms made of natural rubber latex without spermicidal lubricant. FDA has prepared this Small Entity Compliance Guide in accordance with section 212 of the Small Business Regulatory Enforcement Fairness Act of 1996 (Public Law 104-121). This guide is intended to provide guidance to small businesses on the requirements of Title 21, Code of Federal Regulations, amended Section 884.5300.
Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)
If unable to submit comments online, please mail written comments to:
Division of Dockets Management (HFA- 305)
Food and Drug Administration
5630 Fishers Lane, Rm. 1061
Rockville, MD 20852
All comments should be identified with the title of the guidance.