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

AIA-PACK CTNI 2ND-GEN ASSAY

K Number: K012820 · Decision Dec 14, 2001
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
94
Applicant Total
41
Review Days
113

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Basic Information

Device Name
AIA-PACK CTNI 2ND-GEN ASSAY
K Number
K012820
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tosoh Medics, Inc.
Date Received
August 23, 2001
Decision Date
December 14, 2001
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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