# AngioSafe

FEI: 3013757884
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: AngioSafe (#10055439)

Address: 5215 Hellyer Ave Ste 240, San Jose, CA, US



## Products

Total registered: 1
Top product codes: PDU
Regulation §: 870.1250

Proprietary names: Santreva-ATK Endovascular Revascularization Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013757884%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013757884