BEUDAMED
    FDA Registration Active 🇺🇸 United States

    DISPOCAP AIR, 10/PKG (100160)

    Reg #: 2518897 · FEI: 1000080301 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PENTAX of America, Inc.
    Registration Number
    2518897
    FEI Number
    1000080301
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    3 Paragon Drive
    City
    MONTVALE
    State
    NJ
    ZIP
    07645
    Country
    US

    Regulatory Submissions

    510(k) Number
    K093665

    Owner / Operator

    Firm Name
    HOYA Corporation PENTAX Division
    Operator Number
    8030235
    Address
    3 Paragon Drive
    City
    Montvale
    State
    NJ
    Postal Code
    07645
    Country
    US
    Correspondent
    Gurvinder Nanda

    Products

    Device Name Product Code
    Cystoscope And Accessories, Flexible/Rigid FAJ

    Proprietary Names

    DISPOCAP AIR, 10/PKG (100160) CO2 TUBING EGA-501 10/PKG (100551) DISPOCAP CO2, 10/PKG (100150CO2)

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198