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
1580592470
Device Listing 1580592470
Listing Summary
#
Listing key
1580592470
Premarket submission
K120107
Device
SCKOONCUP
Applicant
Sckoon, Inc.
Product code
HHE
Decision date
2012-09-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
146337
3009843022
3009843022
SCKOON INC
1
N
2020-04-25
2301 Collins ave #310 Miami Beach FL US 33139