Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1374856796
Device Listing 1374856796
Listing Summary
#
Listing key
1374856796
Premarket submission
K951595
Device
ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES
Applicant
Roche Diagnostic Systems, Inc.
Product code
CGX
Decision date
1995-09-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
134960
3006198300
3006198300
Kathy Fisher
1
N
2026-01-01
333 Fiske St Holliston MA US 01746