SYNERMED URIC ACID REAGENT KIT— 510(k) K903727

Substantially Equivalent

Synermed, Inc.

FDA 510(k) clearance K903727 for SYNERMED URIC ACID REAGENT KIT, Substantially Equivalent on 1990-09-27. Applicant: Synermed, Inc.. Device class: 1.

Clearance details

Applicant: Synermed, Inc.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1990-08-16
Decision date: 1990-09-27
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.

K973109 — SYNERMED NEAR-INFRARED DIRECT BILIRUBIN REAGENT KIT1997-09-25
K972716 — SYNERMED TOTAL BILIRUBIN REAGENT KIT1997-08-07
K971491 — SYNERMED IR 200 CHEMISTRY ANALYZER1997-06-26
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.