K-number	K931986
Device name	AMP ALKALINE PHOSPHATASE REAGENT KIT
Applicant	Synermed, Inc.
Product code	CJE
Device class	Class II
Decision date	Sep 8, 1993
Decision	Substantially Equivalent
Regulation	862.1050

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View the full FDA submission: accessdata.fda.gov

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AMP ALKALINE PHOSPHATASE REAGENT KIT

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