510(k) K222881

Device
Access hsTnI
Applicant
Beckman Coulter, Inc.
510(k) number
K222881
Product code
MMI
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-18
Date received
2022-09-22
Regulation
862.1215
Classification name
Immunoassay Method, Troponin Subunit
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Kate Oelberg
Address
1000 Lake Hazeltine Dr. Chaska MN US 55318 55318

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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