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

V-TREND TARGET CRP TEST

K Number: K890423 · Decision Feb 17, 1989
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
27
Review Days
22

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Basic Information

Device Name
V-TREND TARGET CRP TEST
K Number
K890423
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Texas Immunology, Inc.
Date Received
January 26, 1989
Decision Date
February 17, 1989
Product Code
DCK
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
DCK C-Reactive Protein, Antigen, Antiserum, And Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DCK), ordered by most recent decision date.

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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
K904105 V-TREND TARGET RF TEST
K892231 V-TREND TARGET CRP TEST
K890041 V-TREND TARGET IM TEST
Search all 27 clearances from Texas Immunology, Inc. →