K-number	K811832
Device name	PRECINORM U & PRECIPATH U HUMAN SERUM
Applicant	Boehringer Mannheim Corp.
Product code	JJX
Device class	Class I
Decision date	Jul 15, 1981
Decision	Substantially Equivalent
Regulation	862.1660

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View the full FDA submission: accessdata.fda.gov

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PRECINORM U & PRECIPATH U HUMAN SERUM

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