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
1318590962
Device Listing 1318590962
Listing Summary
#
Listing key
1318590962
Premarket submission
K083021
Device
APEX HP M PH.I.S.I.O. ADULT HOLLOW FIBER MEMBRANE OXYGENATOR
Applicant
Sorin Group Italia S.R.L.
Product code
DTZ
Decision date
2008-10-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
176608
3006948478
3006948478
STERIS SPA
1
N
2020-04-25
via A. Piva Poggio Rusco Mantova IT 46025