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
1106603572
Device Listing 1106603572
Listing Summary
#
Listing key
1106603572
Premarket submission
K171290
Device
Vela RX PTA Balloon Dilatation Catheter
Applicant
Curatia Medical
Product code
LIT
Decision date
2017-07-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
114505
3008261722
3008261722
Jason Sun
1
N
2026-01-01
830 Stewart Drive Sunnyvale CA US 94085
114509
3008361782
3008361782
Curatia Medical Co.
1
Y
2026-01-01
830 Stewart Drive Sunnyvale CA US 94085