BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AngioSafe

    Reg #: 3013757884 · FEI: 3013757884 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    AngioSafe
    Registration Number
    3013757884
    FEI Number
    3013757884
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    5215 Hellyer Ave Ste 240
    City
    San Jose
    State
    CA
    ZIP
    95138
    Country
    US

    Regulatory Submissions

    510(k) Number
    K252315

    Owner / Operator

    Firm Name
    AngioSafe
    Operator Number
    10055439
    Address
    6150 Hellyer Avenue
    City
    San Jose
    State
    CA
    Postal Code
    95138
    Country
    US

    Products

    Device Name Product Code
    Catheter For Crossing Total Occlusions PDU

    Proprietary Names

    Santreva-ATK Endovascular Revascularization Catheter

    Establishment Types

    Manufacture Medical Device