Cholesterol Reagent

FDA 510(k) K823500 · Ac Biochemical Laboratories, Inc.

Substantially Equivalent

510(k) numberK823500

Submission

Device name
Cholesterol Reagent
Applicant
Ac Biochemical Laboratories, Inc.
Walker, MI, US
Received
November 24, 1982
Decision date
December 30, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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More from Axis-Shield Poc AS

510(k)DeviceDecision
K823537Glucose ReagentFMF · Traditional 04/06/1983SE
K822913Uric Acid ReagentKNK · Traditional 12/20/1982SE

Questions and answers

When was Cholesterol Reagent cleared by the FDA?

Cholesterol Reagent (K823500) received a 510(k) decision of Substantially Equivalent on December 30, 1982, 36 days after the submission was received.

What is the product code of K823500?

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