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
1443001560
Device Listing 1443001560
Listing Summary
#
Listing key
1443001560
Premarket submission
K170175
Device
ENDOSEAL MTA
Applicant
Maruchi
Product code
KIF
Decision date
2018-02-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13207
8030938
3004586882
DIRECTA AB
1
N
2027-01-01
PO BOX 723 FINVIDS VAG 8 UPPLANDS VAESBY Stockholm SE 194 27