CREATININE-PO REAGENT KIT— 510(k) K943924

Substantially Equivalent

Synermed, Inc.

FDA 510(k) clearance K943924 for CREATININE-PO REAGENT KIT, Substantially Equivalent on 1994-09-20. Applicant: Synermed, Inc.. Device class: 2.

Clearance details

Applicant: Synermed, Inc.
Product code: Code CGX
Device class: Class 2
Regulation: 21 CFR 862.1225
Advisory panel: Clinical Chemistry
Date received: 1994-08-12
Decision date: 1994-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Quebec, Canada, CA

Download summary PDF View on FDA.gov ↗

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More clearances from Synermed, Inc.

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K962479 — SYNERMED ISE REAGENTS1997-03-03
K963939 — SYNERMED DIRECT BILIRUBIN REAGENT KIT1996-12-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.