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

QUIKPAC II ONE STEP BENZODIAZEPINE TEST

K Number: K973326 · Decision Feb 24, 1998
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
89
Applicant Total
13
Review Days
173

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Basic Information

Device Name
QUIKPAC II ONE STEP BENZODIAZEPINE TEST
K Number
K973326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3170
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Drial Consultants, Inc.
Date Received
September 4, 1997
Decision Date
February 24, 1998
Product Code
JXM
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
JXM Enzyme Immunoassay, Benzodiazepine

Similar 510(k) Clearances

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

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Other Clearances by Drial Consultants, Inc.

K Number Device Name
K973269 QUIKSTRIP ONE STEP BENZODIAZEPINE TEST
K973047 ONE STEP URINE DRUG OF ABUSE BARBITURATE TEST
K972059 QUIKPAC II ONE STEP COCAINE 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. →