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
1843559762
Device Listing 1843559762
Listing Summary
#
Listing key
1843559762
Premarket submission
K220903
Device
WebCeph
Applicant
Assemblecircle Corp.
Product code
LLZ
Decision date
2022-08-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
308333
3023702877
3023702877
ASSEMBLECIRCLE CORP.
1
N
2026-01-01
R02-ho, 8th floor, 12, Daewangpangyo-ro 645beon-gil, Bundang-gu Seongnam-si Gyeonggi KR 13487