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

QUICKSCREEN COCAINE 150 SCREENING TEST

K Number: K103295 · Decision Feb 1, 2012
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
15
Review Days
450

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Basic Information

Device Name
QUICKSCREEN COCAINE 150 SCREENING TEST
K Number
K103295
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Phamatech, Inc.
Date Received
November 8, 2010
Decision Date
February 1, 2012
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

Similar 510(k) Clearances

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

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Other Clearances by Phamatech, Inc.

K Number Device Name
K181945 QuickScreen Pro Multi Drug Screening Test, Model 9395Z
K131069 QUICKSCREEN AMPHETINE 500 TEST
K070009 AT HOME DRUG TEST MODELS, 9308T AND 9308X
K070098 QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC
K043599 MOMENTS MENOPAUSE CHECK, MODEL 9113
K043051 QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121
K043167 PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T AND 9195X
K040575 PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112
K021409 AT HOME OVULATION TEST, MODEL 9032
K013408 AT HOME DRUG TEST, MODEL 9079
Search all 15 clearances from Phamatech, Inc. →