Triglyceride (Gpo-Trinder) Reagent

FDA 510(k) K870012 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK870012

Submission

Device name
Triglyceride (Gpo-Trinder) Reagent
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
January 2, 1987
Decision date
February 20, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

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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

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Questions and answers

When was Triglyceride (Gpo-Trinder) Reagent cleared by the FDA?

Triglyceride (Gpo-Trinder) Reagent (K870012) received a 510(k) decision of Substantially Equivalent on February 20, 1987, 49 days after the submission was received.

What is the product code of K870012?

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