Synermed Amylase Reagent Kit

FDA 510(k) K941091 · Synermed, Inc.

Substantially Equivalent

510(k) numberK941091

Submission

Device name
Synermed Amylase Reagent Kit
Applicant
Synermed, Inc.
Quebec, Canada, CA
Received
March 8, 1994
Decision date
May 3, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JFJ – Catalytic Methods, Amylase
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1070
Specialty
Clinical Chemistry

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Questions and answers

When was Synermed Amylase Reagent Kit cleared by the FDA?

Synermed Amylase Reagent Kit (K941091) received a 510(k) decision of Substantially Equivalent on May 3, 1994, 56 days after the submission was received.

What is the product code of K941091?

The FDA product code is JFJ – Catalytic Methods, Amylase, a Class II (moderate risk) device regulated under 21 CFR 862.1070.