Bayer Diagnostics ACS:180 and Advia Centaur Troponin I Assay

FDA 510(k) K993309 · Bayer Corp.

Substantially Equivalent

510(k) numberK993309

Submission

Device name
Bayer Diagnostics ACS:180 and Advia Centaur Troponin I Assay
Applicant
Bayer Corp.
Medfield, MA, US
Received
October 4, 1999
Decision date
December 6, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MMI – Immunoassay Method, Troponin Subunit
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1215
Specialty
Clinical Chemistry

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K241165Atellica® IM High-Sensitivity Troponin I (TnIH)MMI · Traditional Siemens Healthcare Diagnostics, Inc.07/25/2024SE
K231974PATHFAST®hs-cTnI-IIMMI · Traditional Phc Corporation03/20/2024SE
K222881Access hsTnIMMI · Traditional Beckman Coulter, Inc.12/18/2023SE
K230648Access hsTnIMMI · Traditional Beckman Coulter, Inc.12/04/2023SE
K230994Alinity i STAT High Sensitivity Troponin-IMMI · Special Abbott Laboratories Diagnostics Division05/04/2023SE

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K021428Clinitek Atlas Pro 12 Reagent Pak SystemJFY · Traditional 07/05/2002SE
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Questions and answers

When was Bayer Diagnostics ACS:180 and Advia Centaur Troponin I Assay cleared by the FDA?

Bayer Diagnostics ACS:180 and Advia Centaur Troponin I Assay (K993309) received a 510(k) decision of Substantially Equivalent on December 6, 1999, 63 days after the submission was received.

What is the product code of K993309?

The FDA product code is MMI – Immunoassay Method, Troponin Subunit, a Class II (moderate risk) device regulated under 21 CFR 862.1215.