BEUDAMED
    FDA Registration Active 🇺🇸 United States

    KSEA CLEARVISION II, MODEL 40334120

    Reg #: 3010202439 · FEI: 3007475226 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Karl Storz Endoscopy-America, Inc.
    Registration Number
    3010202439
    FEI Number
    3007475226
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2151 E. Grand Avenue
    City
    El Segundo
    State
    CA
    ZIP
    90245
    Country
    US

    Regulatory Submissions

    510(k) Number
    K072410

    Owner / Operator

    Firm Name
    KARL STORZ SE & CO KG
    Operator Number
    8010119
    Address
    Dr.-Karl-Storz-Strasse 34,
    City
    TUTTLINGEN
    State
    Baden-Wurttemberg
    Postal Code
    78532
    Country
    DE

    Products

    Device Name Product Code
    Endoscope, Neurological GWG

    Proprietary Names

    KSEA CLEARVISION II, MODEL 40334120

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198