FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VITROS Immunodiagnostic Products hs Troponin I Reagent Pack

K Number: K252393 · Decision Oct 29, 2025
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
94
Applicant Total
106
Review Days
90

Basic Information

Device Name
VITROS Immunodiagnostic Products hs Troponin I Reagent Pack
K Number
K252393
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho-Clinical Diagnostics, Inc.
Date Received
July 31, 2025
Decision Date
October 29, 2025
Product Code
MMI
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MMI Immunoassay Method, Troponin Subunit

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