Direct HDL Cholesterol (HDL)

FDA 510(k) K153435 · Randox Laboratories, Ltd.

Substantially Equivalent

510(k) numberK153435

Submission

Device name
Direct HDL Cholesterol (HDL)
Applicant
Randox Laboratories, Ltd.
Crumlin, GB
Received
November 27, 2015
Decision date
January 8, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LBS – Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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Questions and answers

When was Direct HDL Cholesterol (HDL) cleared by the FDA?

Direct HDL Cholesterol (HDL) (K153435) received a 510(k) decision of Substantially Equivalent on January 8, 2016, 42 days after the submission was received.

What is the product code of K153435?

The FDA product code is LBS – Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl, a Class I (low risk) device regulated under 21 CFR 862.1475.