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

V-TREND TARGET RF TEST

K Number: K904105 · Decision Oct 15, 1990
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
27
Review Days
39

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Basic Information

Device Name
V-TREND TARGET RF TEST
K Number
K904105
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Texas Immunology, Inc.
Date Received
September 6, 1990
Decision Date
October 15, 1990
Product Code
DHR
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
DHR System, Test, Rheumatoid Factor

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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
K963680 TARGET MYOGLOBIN TEST
K912246 TARGET MICROALBUMINURIA TEST
K910073 TARGET ASO 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. →