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
1090117315
Device Listing 1090117315
Listing Summary
#
Listing key
1090117315
Premarket submission
K130501
Device
INTENSIF
Applicant
Endymed Medical, Ltd.
Product code
OUH
Decision date
2014-03-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
111146
3008085016
3008085016
Yong Sun
1
N
2027-01-01
2500 Bee Caves Rd Ste 1 Ste 300 Austin TX US 78746