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
1287507284
Device Listing 1287507284
Listing Summary
#
Listing key
1287507284
Premarket submission
K221811
Device
Vista BC Sealer
Applicant
Inter-Med, Inc.
Product code
KIF
Decision date
2022-11-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
52282
2133714
3000209941
INTER-MED, INC.
1
N
2026-01-01
2200 South St Racine WI US 53404