Beckman Total Bilirubin Triggered (Tb-T) Kit

FDA 510(k) K902801 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK902801

Submission

Device name
Beckman Total Bilirubin Triggered (Tb-T) Kit
Applicant
Beckman Instruments, Inc.
Brea, CA, US
Received
June 27, 1990
Decision date
July 17, 1990
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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Questions and answers

When was Beckman Total Bilirubin Triggered (Tb-T) Kit cleared by the FDA?

Beckman Total Bilirubin Triggered (Tb-T) Kit (K902801) received a 510(k) decision of Substantially Equivalent on July 17, 1990, 20 days after the submission was received.

What is the product code of K902801?

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