Il Test Amylase

FDA 510(k) K974125 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK974125

Submission

Device name
Il Test Amylase
Applicant
Instrumentation Laboratory CO
Lexington, MA, US
Received
November 3, 1997
Decision date
December 17, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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 Il Test Amylase cleared by the FDA?

Il Test Amylase (K974125) received a 510(k) decision of Substantially Equivalent on December 17, 1997, 44 days after the submission was received.

What is the product code of K974125?

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