Roche Diagnostics, Boehringer Mannheim Corporation Liquid Direct Bilirubin Reagent, Catalog Number 1877844

FDA 510(k) K981883 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK981883

Submission

Device name
Roche Diagnostics, Boehringer Mannheim Corporation Liquid Direct Bilirubin Reagent, Catalog Number 1877844
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
May 29, 1998
Decision date
July 7, 1998
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 Roche Diagnostics, Boehringer Mannheim Corporation Liquid Direct Bilirubin Reagent, Catalog Number 1877844 cleared by the FDA?

Roche Diagnostics, Boehringer Mannheim Corporation Liquid Direct Bilirubin Reagent, Catalog Number 1877844 (K981883) received a 510(k) decision of Substantially Equivalent on July 7, 1998, 39 days after the submission was received.

What is the product code of K981883?

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