Cholestech Lipid Monitoring Sys.

FDA 510(k) K912136 · Cholestech Corp.

Substantially Equivalent

510(k) numberK912136

Submission

Device name
Cholestech Lipid Monitoring Sys.
Applicant
Cholestech Corp.
Hayward, CA, US
Received
May 14, 1991
Decision date
July 30, 1991
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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K946066Total Cholesterol, HDL Cholesterol and Glucose PanelCHH · Traditional 02/22/1995SE
K946065Total Cholesterolm HDL Cholesterol and Triglycerides PanelCHH · Traditional 02/22/1995SE
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Questions and answers

When was Cholestech Lipid Monitoring Sys. cleared by the FDA?

Cholestech Lipid Monitoring Sys. (K912136) received a 510(k) decision of Substantially Equivalent on July 30, 1991, 77 days after the submission was received.

What is the product code of K912136?

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