Carolina Liquid Chemistries HDL Cholesterol Reagent

FDA 510(k) K132711 · Carolina Liquid Chemistries Corp.

Substantially Equivalent

510(k) numberK132711

Submission

Device name
Carolina Liquid Chemistries HDL Cholesterol Reagent
Applicant
Carolina Liquid Chemistries Corp.
Winston-Salem, NC, US
Received
August 29, 2013
Decision date
May 8, 2014
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 Carolina Liquid Chemistries HDL Cholesterol Reagent cleared by the FDA?

Carolina Liquid Chemistries HDL Cholesterol Reagent (K132711) received a 510(k) decision of Substantially Equivalent on May 8, 2014, 252 days after the submission was received.

What is the product code of K132711?

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.