SYNERMED PHOSPHORUS REAGENT KIT— 510(k) K912569

Substantially Equivalent

Synermed, Inc.

FDA 510(k) clearance K912569 for SYNERMED PHOSPHORUS REAGENT KIT, Substantially Equivalent on 1991-07-17. Applicant: Synermed, Inc.. Device class: 1.

Clearance details

Applicant: Synermed, Inc.
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1991-06-11
Decision date: 1991-07-17
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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K963939 — SYNERMED DIRECT BILIRUBIN REAGENT KIT1996-12-18

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