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

QUIKPAC II ONE STEP COCAINE TEST

K Number: K972059 · Decision Aug 28, 1997
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
13
Review Days
87

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Basic Information

Device Name
QUIKPAC II ONE STEP COCAINE TEST
K Number
K972059
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Drial Consultants, Inc.
Date Received
June 2, 1997
Decision Date
August 28, 1997
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

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Other Clearances by Drial Consultants, Inc.

K Number Device Name
K973269 QUIKSTRIP ONE STEP BENZODIAZEPINE TEST
K973326 QUIKPAC II ONE STEP BENZODIAZEPINE TEST
K973047 ONE STEP URINE DRUG OF ABUSE BARBITURATE TEST
K972571 QUIKSTRIP ONE STEP OPIATES TEST
K972405 QUIKPAC II ONE STEP OPIATE TEST
K971926 QUIKSTRIP ONE STEP COCAINE TEST
K970395 QUIKSTRIP ONE STEP METHAMPHETAMINE
K971218 QUIKSTRIP ONE STEP AMPHETAMINE TEST
K971109 QUIKPAC II ONE STEP AMPHETAMINE TEST
K970724 QUICKPAC II ONE STEP METHAMPHETAMINE TEST
Search all 13 clearances from Drial Consultants, Inc. →