K-number	K896954
Device name	ABBOTT SPECTRUM URIC ACID REAGENT KIT
Applicant	Abbott Laboratories
Product code	KNK
Device class	Class I
Decision date	Feb 23, 1990
Decision	Substantially Equivalent
Regulation	862.1775

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View the full FDA submission: accessdata.fda.gov

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ABBOTT SPECTRUM URIC ACID REAGENT KIT

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