Dri-Stat Enzymatic Bilirubin Reagent, Synchron Systems Bilirubin Calibrator

FDA 510(k) K053090 · Beckman Coulter, Inc.

Substantially Equivalent

510(k) numberK053090

Submission

Device name
Dri-Stat Enzymatic Bilirubin Reagent, Synchron Systems Bilirubin Calibrator
Applicant
Beckman Coulter, Inc.
Brea, CA, US
Received
November 2, 2005
Decision date
December 16, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JFM – Enzymatic Method, Bilirubin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1110
Specialty
Clinical Chemistry

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K063845Advia Chemistry Total BILIRUBIN_2JFM · Traditional Bayer Healthcare, LLC12/07/2007SE
K053132Wako Direct Bilirubin V, Models 996-23591, 412-22901, 992-23691, 998-23791JFM · Traditional Wako Chemicals USA, Inc.12/30/2005SE
K053131Wako Total Bilirubin V, Models 410-22701, 998-23291, 416-22801, 990-23191JFM · Traditional Wako Chemicals USA, Inc.12/30/2005SE
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K970985Wako Total Bilirubin VJFM · Traditional Wako Chemicals USA, Inc.04/21/1997SE
K904660Enzymatic Bilirubin (Total), Catalogue No. 202-14JFM · Traditional Diagnostic Chemicals, Ltd. (Usa)11/20/1990SE
K843174Dri-Stat Enzymatic Bilirubin Test KitJFM · Traditional Beckman Instruments, Inc.09/14/1984SE

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Questions and answers

When was Dri-Stat Enzymatic Bilirubin Reagent, Synchron Systems Bilirubin Calibrator cleared by the FDA?

Dri-Stat Enzymatic Bilirubin Reagent, Synchron Systems Bilirubin Calibrator (K053090) received a 510(k) decision of Substantially Equivalent on December 16, 2005, 44 days after the submission was received.

What is the product code of K053090?

The FDA product code is JFM – Enzymatic Method, Bilirubin, a Class II (moderate risk) device regulated under 21 CFR 862.1110.