Triglycerides

FDA 510(k) K150819 · Randox Laboratories Limited

Substantially Equivalent

510(k) numberK150819

Submission

Device name
Triglycerides
Applicant
Randox Laboratories Limited
Crumlin, GB
Received
March 27, 2015
Decision date
August 6, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CDT – Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides
Device class
Class I (low risk)
Regulation
21 CFR 862.1705
Specialty
Clinical Chemistry

Other 510(k)s with product code CDT

510(k)DeviceApplicantDecision
K133067Advia Chemistry TRIGLYCERIDES_2 (TRIG_2) ReagentCDT · Traditional Siemens Healthcare Diagnostics, Inc.11/22/2013SE
K130332Vitros Chemistry Products Trig SlidesCDT · Special Ortho-Clinical Diagnostics, Inc.05/31/2013SE
K113830Vantera Clinical AnalyzerCDT · Traditional Liposcience08/30/2012SE
K102993Elitech Clinical Systems Triglycerides SL, Elitech Clinical Systems Cholesterol SLCDT · Traditional Seppim S.A.S.05/19/2011SE
K063804Olympus Triglyceride Test SystemCDT · Traditional Olympus America, Inc.03/23/2007SE
K043546Dimension RXL Max with Streamlab Analytical Workcell and Sample Transfer ModuleCDT · Special Dade Behring, Inc.01/18/2005SE
K034000Vitalab Triglycerides Reagent and Vitalab CalibratorCDT · Traditional Clinical Data, Inc.03/10/2004SE
K020488Careside TrglycerideCDT · Traditional Careside, Inc.04/15/2002SE
K010871TGL Flex Reagent CartridgeCDT · Traditional Dade Behring, Inc.07/09/2001SE
K993466Wako L-Type Triglyceride TestCDT · Traditional Wako Chemicals USA, Inc.11/09/1999SE

More from Wako Chemicals USA, Inc.

510(k)DeviceDecision
K250741Evidence MultiSTAT DOA Urine MultiPlexDJG · Traditional 01/23/2026SE
K221550Evidence MultiSTAT DOA Urine MultiPlexDJG · Traditional 10/05/2023SE
K220451Evidence MultiSTAT DOA Urine MultiPlex, Evidence MultiSTATDJG · Traditional 10/05/2023SE
K230890ISE ElectrodesCEM · Special 09/08/2023SE
K182042Randox Calcium (Ca)CJY · Traditional 10/23/2018SE
K162200Randox RX Daytona Plus Magnesium (MG)JGJ · Traditional 04/28/2017SE
K162275Randox RX Daytona Plus Alkaline Phosphatase (ALP)CJE · Traditional 04/21/2017SE
K161691Direct LDL Cholesterol (LDL)MRR · Traditional 03/20/2017SE
K152085Liquid CO2-2 (LCO2-2)KHS · Traditional 02/24/2016SE
K152343Direct BilirubinJFM · Traditional 02/16/2016SE

Questions and answers

When was Triglycerides cleared by the FDA?

Triglycerides (K150819) received a 510(k) decision of Substantially Equivalent on August 6, 2015, 132 days after the submission was received.

What is the product code of K150819?

The FDA product code is CDT – Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides, a Class I (low risk) device regulated under 21 CFR 862.1705.