(SKD) Cholesterol Test Kit

FDA 510(k) K875131 · Smithkline Diagnostics, Inc.

Substantially Equivalent

510(k) numberK875131

Submission

Device name
(SKD) Cholesterol Test Kit
Applicant
Smithkline Diagnostics, Inc.
Sunnyvale, CA, US
Received
December 15, 1987
Decision date
March 1, 1988
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 (SKD) Cholesterol Test Kit cleared by the FDA?

(SKD) Cholesterol Test Kit (K875131) received a 510(k) decision of Substantially Equivalent on March 1, 1988, 77 days after the submission was received.

What is the product code of K875131?

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