FDA.reportPublic FDA data

AngioSafe

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30137578843013757884AngioSafe1N2026-01-015215 Hellyer Ave Ste 240 San Jose CA US 95138
30137578843013757884ANGIOSAFE1N2020-04-256150 Hellyer Avenue Suite 150 San Jose CA US 95138

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3367062063788779K252315Santreva™-ATK Endovascular Revasculariztion CatheterPDU2025-09-22
2098772038976038

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PDU12025-09-22

PMN#

GUDID#