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

COBAS INTEGRA CARBON DIOXIDE (CO2-S), COBAS INTEGRA GLUCOSE HK LIQUID (GLULF)

K Number: K980996 · Decision Jun 5, 1998
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
85
Applicant Total
296
Review Days
80

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
COBAS INTEGRA CARBON DIOXIDE (CO2-S), COBAS INTEGRA GLUCOSE HK LIQUID (GLULF)
K Number
K980996
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1160
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Roche Diagnostic Systems, Inc.
Date Received
March 17, 1998
Decision Date
June 5, 1998
Product Code
KHS
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
KHS Enzymatic, Carbon-Dioxide

Similar 510(k) Clearances

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

View all

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
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
Search all 296 clearances from Roche Diagnostic Systems, Inc. →