Iq/Qca Total Bilirubin

FDA 510(k) K874261 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK874261

Submission

Device name
Iq/Qca Total Bilirubin
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lakes, NJ, US
Received
October 20, 1987
Decision date
November 25, 1987
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

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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
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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

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Questions and answers

When was Iq/Qca Total Bilirubin cleared by the FDA?

Iq/Qca Total Bilirubin (K874261) received a 510(k) decision of Substantially Equivalent on November 25, 1987, 36 days after the submission was received.

What is the product code of K874261?

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