Direct Bilirubin Liquicolor and Total Bilirubin Liquicolor

FDA 510(k) K050266 · Stanbio Laboratory

Substantially Equivalent

510(k) numberK050266

Submission

Device name
Direct Bilirubin Liquicolor and Total Bilirubin Liquicolor
Applicant
Stanbio Laboratory
Boerne, TX, US
Received
February 4, 2005
Decision date
June 30, 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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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
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K843174Dri-Stat Enzymatic Bilirubin Test KitJFM · Traditional Beckman Instruments, Inc.09/14/1984SE

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Questions and answers

When was Direct Bilirubin Liquicolor and Total Bilirubin Liquicolor cleared by the FDA?

Direct Bilirubin Liquicolor and Total Bilirubin Liquicolor (K050266) received a 510(k) decision of Substantially Equivalent on June 30, 2005, 146 days after the submission was received.

What is the product code of K050266?

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