Diazo Colorimetry, Billirubin

FDA 510(k) K832870 · Pointe Scientific, Inc.,

Substantially Equivalent

510(k) numberK832870

Submission

Device name
Diazo Colorimetry, Billirubin
Applicant
Pointe Scientific, Inc.,
Mchenry, IL, US
Received
August 25, 1983
Decision date
September 26, 1983
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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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
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Questions and answers

When was Diazo Colorimetry, Billirubin cleared by the FDA?

Diazo Colorimetry, Billirubin (K832870) received a 510(k) decision of Substantially Equivalent on September 26, 1983, 32 days after the submission was received.

What is the product code of K832870?

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