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
1768992439
Device Listing 1768992439
Listing Summary
#
Listing key
1768992439
Premarket submission
K073543
Device
OEC 9900 ELITE
Applicant
Ge Oec Medical Systems
Product code
OWB
Decision date
2008-05-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
223227
3007562060
3007562060
Martin Pedroza
1
N
2020-04-25
100 Park Avenue Suite 300 Orange Village OH US 44122