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

ABUSCREEN FP FOR COCAINE METABOLITE

K Number: K890885 · Decision Mar 13, 1989
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
144
Applicant Total
296
Review Days
20

Basic Information

Device Name
ABUSCREEN FP FOR COCAINE METABOLITE
K Number
K890885
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Date Received
February 21, 1989
Decision Date
March 13, 1989
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

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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. →