Olympus Cholesterol Reagent

FDA 510(k) K922231 · Olympus Corp.

Substantially Equivalent

510(k) numberK922231

Submission

Device name
Olympus Cholesterol Reagent
Applicant
Olympus Corp.
Lake Success, NY, US
Received
May 12, 1992
Decision date
November 18, 1992
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 Olympus Cholesterol Reagent cleared by the FDA?

Olympus Cholesterol Reagent (K922231) received a 510(k) decision of Substantially Equivalent on November 18, 1992, 190 days after the submission was received.

What is the product code of K922231?

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