K-number	K991800
Device name	HEMOCHEK URINE COLLECTION KIT
Applicant	Osborn Group, Inc.
Product code	JIQ
Device class	Class I
Decision date	Sep 24, 1999
Decision	Substantially Equivalent
Regulation	862.1645

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View the full FDA submission: accessdata.fda.gov

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HEMOCHEK URINE COLLECTION KIT

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