Wiener Lab. Bilirubina Direct Aa

FDA 510(k) K024116 · Wiener Laboratories Saic

Substantially Equivalent

510(k) numberK024116

Submission

Device name
Wiener Lab. Bilirubina Direct Aa
Applicant
Wiener Laboratories Saic
Rosario, Santa Fe, AR
Received
December 13, 2002
Decision date
February 12, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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 Wiener Lab. Bilirubina Direct Aa cleared by the FDA?

Wiener Lab. Bilirubina Direct Aa (K024116) received a 510(k) decision of Substantially Equivalent on February 12, 2003, 61 days after the submission was received.

What is the product code of K024116?

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