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
1337987197
Device Listing 1337987197
Listing Summary
#
Listing key
1337987197
Premarket submission
K192083
Device
Okami Medical LOBO Vascular Occlusion System
Applicant
Okami Medical
Product code
KRD
Decision date
2019-10-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
235810
3016444913
3016444913
Okami Medical Inc.
1
N
2026-01-01
8 Argonaut Suite 100 Aliso Viejo CA US 92656