Ub Analyzer, Model UA-1/REAGENT Kit/Bilirubin Con.

FDA 510(k) K871115 · Labo Science-USA, Inc.

Substantially Equivalent

510(k) numberK871115

Submission

Device name
Ub Analyzer, Model UA-1/REAGENT Kit/Bilirubin Con.
Applicant
Labo Science-USA, Inc.
Briarcliff Manor, NY, US
Received
March 19, 1987
Decision date
January 27, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIG – Diazo Colorimetry, Bilirubin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1110
Specialty
Clinical Chemistry

Other 510(k)s with product code CIG

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K251998Atellica CH Diazo Total Bilirubin (D_TBil)CIG · Traditional Siemens Healthcare Diagnostics, Inc.02/27/2026SE
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K222104Atellica® CH Diazo Total Bilirubin (D_TBil)CIG · Traditional Siemens Healthcare Diagnostics, Inc.03/20/2023SE
K223324Total Bilirubin2CIG · Traditional Abbott Ireland Diagnostics Division12/29/2022SE
K190807VITROS XT Chemistry Products TBIL-ALKP SlidesCIG · Traditional Ortho-Clinical Diagnostics, Inc.04/26/2019SE
K171401ELITech Clinical Systems BILIRUBIN TOTAL 4+1, ELITech Clinical Systems BILIRUBIN DIRECT…CIG · Traditional Elitechgroup07/11/2017SE
K150510Total BilirubinCIG · Traditional Abbott Laboratories04/02/2015SE
K131544Cobas C Bilirubin Total GEN.3CIG · Traditional Roche Diagnostics07/17/2013SE
K131217S Test Reagent Cartridge Total BilirubinCIG · Traditional Hitachi Chemical Diagnostics, Inc.06/07/2013SE
K123802Easyra Tbil Reagent, Easyra Dbii Reagent, Easyra CK ReagentCIG · Traditional Medica Corp.03/01/2013SE

Questions and answers

When was Ub Analyzer, Model UA-1/REAGENT Kit/Bilirubin Con. cleared by the FDA?

Ub Analyzer, Model UA-1/REAGENT Kit/Bilirubin Con. (K871115) received a 510(k) decision of Substantially Equivalent on January 27, 1989, 680 days after the submission was received.

What is the product code of K871115?

The FDA product code is CIG – Diazo Colorimetry, Bilirubin, a Class II (moderate risk) device regulated under 21 CFR 862.1110.