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

TNL-ULTRA ASSAY FOR THE ADVIA CENTAUR SYSTEM

K Number: K053020 · Decision Dec 30, 2005
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
94
Applicant Total
46
Review Days
65

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Basic Information

Device Name
TNL-ULTRA ASSAY FOR THE ADVIA CENTAUR SYSTEM
K Number
K053020
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bayer Healthcare, LLC
Date Received
October 26, 2005
Decision Date
December 30, 2005
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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