K-number	K861831
Device name	REFLOTRON URIC ACID
Applicant	Boehringer Mannheim Corp.
Product code	KNK
Device class	Class I
Decision date	Jul 11, 1986
Decision	Substantially Equivalent
Regulation	862.1775

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View the full FDA submission: accessdata.fda.gov

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REFLOTRON URIC ACID

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