K-number	K790087
Device name	LUBRICANT, OTRHO PERSONAL
Applicant	Ortho Pharmaceutical Corp.
Product code	KMJ
Device class	Class I
Decision date	Feb 1, 1979
Decision	Substantially Equivalent
Regulation	880.6375

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View the full FDA submission: accessdata.fda.gov

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LUBRICANT, OTRHO PERSONAL

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