BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Philips FD20 Cath Lab

    Reg #: 3027373189 · FEI: 3027373189 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    LIBERTY GLOBAL, LLC
    Registration Number
    3027373189
    FEI Number
    3027373189
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    7160 E. Kierland Blvd
    City
    Scottsdale
    State
    AZ
    ZIP
    85254
    Country
    US

    Regulatory Submissions

    510(k) Number
    K033737

    Owner / Operator

    Firm Name
    Liberty Global, LLC
    Operator Number
    10088126
    Address
    7160 E. Kierland Blvd
    City
    Scottsdale
    State
    AZ
    Postal Code
    85254
    Country
    US

    Products

    Device Name Product Code
    Interventional Fluoroscopic X-Ray System OWB
    System, X-Ray, Fluoroscopic, Image-Intensified JAA
    System, X-Ray, Angiographic IZI

    Proprietary Names

    Philips FD20 Cath Lab

    Establishment Types

    Repack or Relabel Medical Device