BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Circul8 Luxe DVT Prevention Device

    Reg #: 3016000973 · FEI: 3016000973 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Precision Medical Products
    Registration Number
    3016000973
    FEI Number
    3016000973
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    3735 Cincinnati Ave Ste 100
    City
    Rocklin
    State
    CA
    ZIP
    95765
    Country
    US

    Regulatory Submissions

    510(k) Number
    K211235

    Owner / Operator

    Firm Name
    Precision Medical Products Inc.
    Operator Number
    10084351
    Address
    2217 Plaza Dr.
    City
    Rocklin
    State
    CA
    Postal Code
    95765
    Country
    US

    Products

    Device Name Product Code
    Sleeve, Limb, Compressible JOW

    Proprietary Names

    Circul8 Luxe DVT Prevention Device

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility