Synermed Albumin Reagent Kit

FDA 510(k) K903543 · Synermed, Inc.

Substantially Equivalent

510(k) numberK903543

Submission

Device name
Synermed Albumin Reagent Kit
Applicant
Synermed, Inc.
Quebec, Canada, CA
Received
August 7, 1990
Decision date
October 12, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIX – Bromcresol Green Dye-Binding, Albumin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1035
Specialty
Clinical Chemistry

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Questions and answers

When was Synermed Albumin Reagent Kit cleared by the FDA?

Synermed Albumin Reagent Kit (K903543) received a 510(k) decision of Substantially Equivalent on October 12, 1990, 66 days after the submission was received.

What is the product code of K903543?

The FDA product code is CIX – Bromcresol Green Dye-Binding, Albumin, a Class II (moderate risk) device regulated under 21 CFR 862.1035.