L.D.X Lipid Monitoring System

FDA 510(k) K901900 · Cholestech Corp.

Substantially Equivalent

510(k) numberK901900

Submission

Device name
L.D.X Lipid Monitoring System
Applicant
Cholestech Corp.
Hayward, CA, US
Received
April 27, 1990
Decision date
July 24, 1990
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 L.D.X Lipid Monitoring System cleared by the FDA?

L.D.X Lipid Monitoring System (K901900) received a 510(k) decision of Substantially Equivalent on July 24, 1990, 88 days after the submission was received.

What is the product code of K901900?

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