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

TARGET MYOGLOBIN TEST

K Number: K963680 · Decision Feb 6, 1997
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
45
Applicant Total
27
Review Days
143

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Basic Information

Device Name
TARGET MYOGLOBIN TEST
K Number
K963680
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5680
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Texas Immunology, Inc.
Date Received
September 16, 1996
Decision Date
February 6, 1997
Product Code
DDR
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DDR Myoglobin, Antigen, Antiserum, Control

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Other Clearances by Texas Immunology, Inc.

K Number Device Name
K991465 DRUG STOP
K980153 DRUG CHECK
K973208 FIRST SIGN
K972094 TARGET CARDIAC TROPONIN I TEST
K912246 TARGET MICROALBUMINURIA TEST
K910073 TARGET ASO TEST
K904105 V-TREND TARGET RF TEST
K892231 V-TREND TARGET CRP TEST
K890423 V-TREND TARGET CRP TEST
K890041 V-TREND TARGET IM TEST
Search all 27 clearances from Texas Immunology, Inc. →