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

Access hsTnl

K Number: K172787 · Decision Jun 14, 2018
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
91
Applicant Total
24
Review Days
272

Basic Information

Device Name
Access hsTnl
K Number
K172787
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beckman Coulter, Inc.
Date Received
September 15, 2017
Decision Date
June 14, 2018
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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