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

ONTRAK TESTSTIK FOR AMPHETAMINES, ONTRAK TESTSTIK FOR COCAINE, ONTRAK TESTSTIK FOR MORPHINE, ONTRAK TESTSTIK FOR PCP, ON

K Number: K973075 · Decision Oct 9, 1997
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
224
Applicant Total
296
Review Days
52

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Basic Information

Device Name
ONTRAK TESTSTIK FOR AMPHETAMINES, ONTRAK TESTSTIK FOR COCAINE, ONTRAK TESTSTIK FOR MORPHINE, ONTRAK TESTSTIK FOR PCP, ON
K Number
K973075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Roche Diagnostic Systems, Inc.
Date Received
August 18, 1997
Decision Date
October 9, 1997
Product Code
DKZ
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
DKZ Enzyme Immunoassay, Amphetamine

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Other Clearances by Roche Diagnostic Systems, Inc.

K Number Device Name
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K983704 MODIFICATION TO ABUSCREEN ONLINE FOR PHENCYCLIDINE
K983556 ABUSCREEN ONLINE BENZ 300 CALIBRATORS
K983555 ABUSCREEN ONLINE BENZ 200 CALIBRATORS
K983697 MODIFICATION TO ABUSCREEN ONLINE COCAINE METABOLITE
K983700 MODIFICATION TO ABUSCREEN ONLINE FOR PROPOXYPHENE
K983701 MODIFICATION TO ABUSCREEN ONLINE FOR CANNABINOIDS
K983699 MODIFICATION TO ABUSCREEN ONLINE FOR AMPHETAMINES
K983703 MODIFICATION TO ABUSCREEN ONLINE FOR METHADONE
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