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

QUICK SCREEN BARBITURATE SCREENING TEST MODELS 9020 AND 9021, QUICK SCREEN PRO MULTI DRUG SCREENING TEST MODL 9152

K Number: K982152 · Decision Sep 21, 1998
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
99
Applicant Total
47
Review Days
95

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Basic Information

Device Name
QUICK SCREEN BARBITURATE SCREENING TEST MODELS 9020 AND 9021, QUICK SCREEN PRO MULTI DRUG SCREENING TEST MODL 9152
K Number
K982152
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3150
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Phamatech
Date Received
June 18, 1998
Decision Date
September 21, 1998
Product Code
DIS
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
DIS Enzyme Immunoassay, Barbiturate

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Other Clearances by Phamatech

K Number Device Name
K041578 QUICKSCREEN, MODELS 9177X AND 9178X
K030447 AT HOME DRUG CUP, MODEL 9150X
K010833 AT WORK DRUG TEST, MODEL 9177T AWT
K010836 AT WORK DRUG TEST, MODEL 9147T AWT
K010654 AT HOME DRUG TEST, MODEL 9078 T
K010653 AT HOME DRUG TEST, MODEL 9068 T
K010655 AT HOME DRUG TESTT, MODEL 9150 T
K010645 AT HOME DRUG TEST, MODEL 9063 T
K010646 AT HOME DRUG TEST, MODEL 9083 T
K010651 AT HOME DRUG TEST, MODEL 9133 T
Search all 47 clearances from Phamatech →