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
1999300409
Device Listing 1999300409
Listing Summary
#
Listing key
1999300409
Premarket submission
K242676
Device
pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device
Applicant
Phenox Limited
Product code
POL
Decision date
2025-02-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
235034
3013656790
3013656790
PHENOX LIMITED
1
N
2026-01-01
Kamrick Court Ballybrit Business Park Galway Galway IE H91XY38