K-number	K921016
Device name	SYNERMED ALT/GPT REAGENT KIT
Applicant	Synermed, Inc.
Product code	CKA
Device class	Class I
Decision date	May 7, 1992
Decision	Substantially Equivalent
Regulation	862.1030

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View the full FDA submission: accessdata.fda.gov

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SYNERMED ALT/GPT REAGENT KIT

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