K-number	K812978
Device name	URIC ACID SYSTEM PACK TEST
Applicant	Boehringer Mannheim Corp.
Product code	KNK
Device class	Class I
Decision date	Nov 6, 1981
Decision	Substantially Equivalent
Regulation	862.1775

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View the full FDA submission: accessdata.fda.gov

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URIC ACID SYSTEM PACK TEST

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