K-number	K872005
Device name	MAXIMUM, LATEX PROPHYLACTIC BRAND
Applicant	Safe Product Supplies
Product code	HIS
Device class	Class II
Decision date	Nov 2, 1987
Decision	Substantially Equivalent
Regulation	884.5300

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View the full FDA submission: accessdata.fda.gov

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MAXIMUM, LATEX PROPHYLACTIC BRAND

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