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
1953472777
Device Listing 1953472777
Listing Summary
#
Listing key
1953472777
Premarket submission
K220566
Device
Vascette HP (hemostatic pad)
Applicant
Koag, LLC
Product code
QSY
Decision date
2022-07-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
296852
3020664666
3020664666
KOAG INTERNATIONAL LLC
1
N
2026-01-01
790 Rarity Bay Parkway Vonore TN US 37885