K-number	K770767
Device name	IN VITRO DIAG. FOR URIC ACID
Applicant	Smithkline Diagnostics, Inc.
Product code	CDO
Device class	Class I
Decision date	Jul 5, 1977
Decision	Substantially Equivalent
Regulation	862.1775

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View the full FDA submission: accessdata.fda.gov

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IN VITRO DIAG. FOR URIC ACID

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