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

DRUG CHECK

K Number: K980153 · Decision Mar 27, 1998
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
27
Review Days
70

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Basic Information

Device Name
DRUG CHECK
K Number
K980153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Texas Immunology, Inc.
Date Received
January 16, 1998
Decision Date
March 27, 1998
Product Code
DIO
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

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Other Clearances by Texas Immunology, Inc.

K Number Device Name
K991465 DRUG STOP
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
K890423 V-TREND TARGET CRP TEST
K890041 V-TREND TARGET IM TEST
Search all 27 clearances from Texas Immunology, Inc. →