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
1005461043
Device Listing 1005461043
Listing Summary
#
Listing key
1005461043
Premarket submission
K220579
Device
Hybrid C70
Applicant
Digimed Co., Ltd.
Product code
EHD
Decision date
2022-09-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
123141
3007933232
3007933232
DIGIMED CO., LTD
1
N
2026-01-01
401, 402, 406~411-ho, A-dong 101, Gasan digital 2-ro, Geumcheon-Gu Seoul KR 08505