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

CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM

K Number: K892060 · Decision Aug 10, 1989
Classifications
1
FEI Numbers
116
Registration Numbers
117
Same Product Code
77
Applicant Total
448
Review Days
134

Basic Information

Device Name
CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM
K Number
K892060
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
SYVA CO.
Date Received
March 29, 1989
Decision Date
August 10, 1989
Product Code
JQP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JQP Calculator/Data Processing Module, For Clinical Use

Similar 510(k) Clearances

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

View all

Other Clearances by SYVA CO.

K Number Device Name
K011878 EMIT (R) TOX SALICYLIC ASSAY, MODEL 7SO19UL, EMIT (R) TOX SALICYLIC ACID CALIBRATORS, MODEL 7S109UL
K012257 EMIT II PLUS MONOCLONAL AMPHETAMINE/METHAMPHETAMINE ASSAY MODEL OSR9C229
K011947 EMIT 2000 VALPROIC ACID ASSAY, MODEL OSR4G229UL
K011528 EMIT 2000 PHENOBARBITAL ASSAY, MODEL OSR4D229
K011347 EMIT 2000 PHENYTOIN ASSAY, MODEL 0SR4A229
K993980 SYVA EMIT II PLUS ETHYL ALCOHOL ASSAY, MODELS 9K309UL/9K409UL
K993981 SYVA EMIT II PLUS PROPOXYPHENE ASSAY, MODELS 9G029UL/9G129UL
K993029 ABBOTT AEROSET THEOPHYLLINE ASSAY AND CALIBRATORS; MODELS 1E09 AND 6E89
K993031 ABBOTT AEROSET PHENOBARBITAL ASSEY AND CALIBRATORS;MODELS 1E08 AND 5F54
K993988 SYVA EMIT II PLUS COCAINE METABOLITE ASSAY, MODEL 9H029UL
Search all 448 clearances from SYVA CO. →