K-number	K092488
Device name	DYNAREX STERILE LUBRICATING JELLY
Applicant	Dynarex Corporation
Product code	KMJ
Device class	Class I
Decision date	Dec 18, 2009
Decision	Substantially Equivalent
Regulation	880.6375

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View the full FDA submission: accessdata.fda.gov

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DYNAREX STERILE LUBRICATING JELLY

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