BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Prowler XS Microcatheter

    Reg #: 3007628272 · FEI: 3007628272 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    Cerenovus, Inc.
    Registration Number
    3007628272
    FEI Number
    3007628272
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    6303 Waterford District Drive, Suites 215 and 315
    City
    Miami
    State
    FL
    ZIP
    33126
    Country
    US

    Regulatory Submissions

    510(k) Number
    K214025

    Owner / Operator

    Firm Name
    Cerenovus, Inc.
    Operator Number
    9026915
    Address
    31 Technology Drive, --
    City
    Irvine
    State
    CA
    Postal Code
    92618
    Country
    US
    Correspondent
    Kevin Leung

    Products

    Device Name Product Code
    Catheter, Continuous Flush KRA
    Catheter, Percutaneous DQY
    Catheter, Percutaneous, Neurovasculature QJP

    Proprietary Names

    Prowler XS Microcatheter Prowler Select LP ES Microcatheter

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility