VITROS XT Chemistry Products TBIL-ALKP Slides

FDA 510(k) K190807 · Ortho-Clinical Diagnostics, Inc.

Substantially Equivalent

510(k) numberK190807

Submission

Device name
VITROS XT Chemistry Products TBIL-ALKP Slides
Applicant
Ortho-Clinical Diagnostics, Inc.
Rochester, NY, US
Received
March 29, 2019
Decision date
April 26, 2019
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 VITROS XT Chemistry Products TBIL-ALKP Slides cleared by the FDA?

VITROS XT Chemistry Products TBIL-ALKP Slides (K190807) received a 510(k) decision of Substantially Equivalent on April 26, 2019, 28 days after the submission was received.

What is the product code of K190807?

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