Dupont Dimension Amylase Method

FDA 510(k) K942640 · Dupont Medical Products

Substantially Equivalent

510(k) numberK942640

Submission

Device name
Dupont Dimension Amylase Method
Applicant
Dupont Medical Products
Wilmington, DE, US
Received
June 3, 1994
Decision date
September 9, 1994
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 Dupont Dimension Amylase Method cleared by the FDA?

Dupont Dimension Amylase Method (K942640) received a 510(k) decision of Substantially Equivalent on September 9, 1994, 98 days after the submission was received.

What is the product code of K942640?

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