Wako(Tm) Autokit Cholesterol

FDA 510(k) K880311 · Wako Chemicals USA, Inc.

Substantially Equivalent

510(k) numberK880311

Submission

Device name
Wako(Tm) Autokit Cholesterol
Applicant
Wako Chemicals USA, Inc.
Dallas, TX, US
Received
January 25, 1988
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 Wako(Tm) Autokit Cholesterol cleared by the FDA?

Wako(Tm) Autokit Cholesterol (K880311) received a 510(k) decision of Substantially Equivalent on March 1, 1988, 36 days after the submission was received.

What is the product code of K880311?

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