K-number	K770272
Device name	URIC ACID TEST, BMC AUTOFLO
Applicant	Boehringer Mannheim Corp.
Product code	KNK
Device class	Class I
Decision date	Mar 1, 1977
Decision	Substantially Equivalent
Regulation	862.1775

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View the full FDA submission: accessdata.fda.gov

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URIC ACID TEST, BMC AUTOFLO

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