FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ABUSCREEN ONTRAK POS.REF.CONTROL FOR PHENCYCLIDINE

K Number: K893860 · Decision Aug 3, 1989
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
82
Applicant Total
296
Review Days
70

Basic Information

Device Name
ABUSCREEN ONTRAK POS.REF.CONTROL FOR PHENCYCLIDINE
K Number
K893860
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Date Received
May 25, 1989
Decision Date
August 3, 1989
Product Code
LAS
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
LAS Drug Specific Control Materials

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Other Clearances by ROCHE DIAGNOSTIC SYSTEMS, INC.

K Number Device Name
K983698 MODIFICATION TO ABUSCREEN ONLINE BARBITURATES
K983702 MODIFICATION TO ABUSCREEN ONLINE FOR BENZOIDIAZEPINES
K983704 MODIFICATION TO ABUSCREEN ONLINE FOR PHENCYCLIDINE
K983556 ABUSCREEN ONLINE BENZ 300 CALIBRATORS
K983555 ABUSCREEN ONLINE BENZ 200 CALIBRATORS
K983700 MODIFICATION TO ABUSCREEN ONLINE FOR PROPOXYPHENE
K983697 MODIFICATION TO ABUSCREEN ONLINE COCAINE METABOLITE
K983699 MODIFICATION TO ABUSCREEN ONLINE FOR AMPHETAMINES
K983703 MODIFICATION TO ABUSCREEN ONLINE FOR METHADONE
K983701 MODIFICATION TO ABUSCREEN ONLINE FOR CANNABINOIDS
Search all 296 clearances from ROCHE DIAGNOSTIC SYSTEMS, INC. →