Cholesterol Test Item# 42374/93, 42322/R1

FDA 510(k) K924508 · Em Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK924508

Submission

Device name
Cholesterol Test Item# 42374/93, 42322/R1
Applicant
Em Diagnostic Systems, Inc.
Gibbstown, NJ, US
Received
September 4, 1992
Decision date
January 28, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CHH – Enzymatic Esterase--Oxidase, Cholesterol
Device class
Class I (low risk)
Regulation
21 CFR 862.1175
Specialty
Clinical Chemistry

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Questions and answers

When was Cholesterol Test Item# 42374/93, 42322/R1 cleared by the FDA?

Cholesterol Test Item# 42374/93, 42322/R1 (K924508) received a 510(k) decision of Substantially Equivalent on January 28, 1993, 146 days after the submission was received.

What is the product code of K924508?

The FDA product code is CHH – Enzymatic Esterase--Oxidase, Cholesterol, a Class I (low risk) device regulated under 21 CFR 862.1175.