Careside Hdl-Cholesterol

FDA 510(k) K981899 · Exigent Diagnostics, Inc.

Substantially Equivalent

510(k) numberK981899

Submission

Device name
Careside Hdl-Cholesterol
Applicant
Exigent Diagnostics, Inc.
Culver City, CA, US
Received
June 1, 1998
Decision date
July 14, 1998
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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K132711Carolina Liquid Chemistries HDL Cholesterol ReagentLBS · Traditional Carolina Liquid Chemistries Corp.05/08/2014SE
K120609Vitros Chemistry Products DHDL SlidesLBS · Special Ortho-Clinical Diagnostics, Inc.09/07/2012SE
K111516NMR Lipoprofile (R) Test and NMR ProfilerLBS · Traditional Liposcience, Inc.09/27/2011SE
K103747Elitech Clincal Systems Cholesterol HDL SL 2G, HDL 2G Calibrator, LDL SL 2G, LDL 2G…LBS · Traditional Elitechgroup Seppim S.A.S.08/31/2011SE
K111036Easyra HDL Reagent; Easyra LDL Reagent; Easyra Chol Reagent; Easyra Trig ReagentLBS · Traditional Medica Corporation07/12/2011SE
K100550Poly-Chem 90 Direct HDL Cholesterol, Poly-Chem 90 Direct LDL Cholesterol, Poly-Chem 90…LBS · Traditional Polymedco, Inc.09/28/2010SE
K100010HDL Cholesterol (HDLX) AssayLBS · Traditional Beckman Coulter, Inc.05/14/2010SE
K080125Apolowako T-Cho, Hdl-C, TG and Analyzer, Models 993-23501, 999-23601, 995-23701 and…LBS · Traditional Wako Chemicals USA, Inc.07/18/2008SE

More from Wako Chemicals USA, Inc.

510(k)DeviceDecision
K982118Careside AnalyzerCHH · Traditional 07/24/1998SE
K981183Careside GlucoseCGA · Traditional 05/07/1998SE
K980043Careside CreatinineJFY · Traditional 03/30/1998SE
K980056Careside AnalyzerJJF · Traditional 03/06/1998SE
K980057Careside BunCDQ · Traditional 02/05/1998SE
K980042Careside Total ProteinCEK · Traditional 02/04/1998SE
K980041Careside AlbuminCIX · Traditional 02/04/1998SE
K980055Careside GlobulinJGE · Traditional 01/28/1998SE

Questions and answers

When was Careside Hdl-Cholesterol cleared by the FDA?

Careside Hdl-Cholesterol (K981899) received a 510(k) decision of Substantially Equivalent on July 14, 1998, 43 days after the submission was received.

What is the product code of K981899?

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.