Enzymatic Cholesterol Kit

FDA 510(k) K843222 · Livonia Diagnostics, Inc.

Substantially Equivalent

510(k) numberK843222

Submission

Device name
Enzymatic Cholesterol Kit
Applicant
Livonia Diagnostics, Inc.
Mchenry, IL, US
Received
August 16, 1984
Decision date
September 28, 1984
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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Questions and answers

When was Enzymatic Cholesterol Kit cleared by the FDA?

Enzymatic Cholesterol Kit (K843222) received a 510(k) decision of Substantially Equivalent on September 28, 1984, 43 days after the submission was received.

What is the product code of K843222?

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