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
1519658526
Device Listing 1519658526
Listing Summary
#
Listing key
1519658526
Premarket submission
K172128
Device
EsoFLIP® ES-310 Balloon Catheter
Applicant
Crospon, Ltd.
Product code
PIE
Decision date
2017-11-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
83898
9681384
3002807626
Kae Miller
1
N
2026-01-01
200 Medtronic Dr Lafayette CO US 80026
140647
3004904811
3004904811
Covidien llc
1
N
2026-01-01
3062 Bunker Hill Lane Santa Clara CA US 95054
81958
3006897778
3006897778
CROSPON LTD.
1
N
2020-04-25
Galway Business Park Dangan Galway Galway IE 00000