Amylase Test

FDA 510(k) K923677 · Em Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK923677

Submission

Device name
Amylase Test
Applicant
Em Diagnostic Systems, Inc.
Gibbstown, NJ, US
Received
July 22, 1992
Decision date
September 9, 1992
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 Amylase Test cleared by the FDA?

Amylase Test (K923677) received a 510(k) decision of Substantially Equivalent on September 9, 1992, 49 days after the submission was received.

What is the product code of K923677?

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