SYNERMED CREATINE KINASE REAGENT KIT— 510(k) K930932

Substantially Equivalent

Synermed, Inc.

FDA 510(k) clearance K930932 for SYNERMED CREATINE KINASE REAGENT KIT, Substantially Equivalent on 1993-05-11. Applicant: Synermed, Inc..

Clearance details

Applicant: Synermed, Inc.
Product code: Code CGS
Advisory panel: Clinical Chemistry
Date received: 1993-02-23
Decision date: 1993-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Quebec, Canada, CA

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