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

BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT

K Number: K013062 · Decision Jan 8, 2002
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
94
Applicant Total
14
Review Days
118

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Basic Information

Device Name
BIOCHECK HUMAN CARDIAC TROPONIN-I IMMUNOASSAY TEST KIT
K Number
K013062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biocheck, Inc.
Date Received
September 12, 2001
Decision Date
January 8, 2002
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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Other Clearances by Biocheck, Inc.

K Number Device Name
K041619 BIO CHECK WHOLE BLOOD/PLASMA/SERMON MODEL #801116
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K022660 BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117
K003851 BIOCHECK HIGH SENSITIVITY C-REACTIVE PROTEIN ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1119
K002294 BIOCHECK TESTOSTERONE EIA, MODEL BC-1115
K001022 BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061
K992517 BIOCHECK FERRITIN ELISA MODEL BC-1025
K992528 BIOCHECK IGE ELISA, MODEL BC-1035
K991741 BIOCHECK HCG ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1027
K991146 TSH ENZYME IMMUNOASSAY TEST KIT, MODEL #BC-1001
Search all 14 clearances from Biocheck, Inc. →