BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Interson SiMPLi Series

    Reg #: 2939830 · FEI: 1000124215 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    3
    Establishment Types
    2
    Classifications
    3

    Registration Details

    Registration Name
    INTERSON CORP.
    Registration Number
    2939830
    FEI Number
    1000124215
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7150 Koll Center Pkwy
    City
    PLEASANTON
    State
    CA
    ZIP
    94566
    Country
    US

    Regulatory Submissions

    510(k) Number
    K163443

    Owner / Operator

    Firm Name
    Interson Corporation
    Operator Number
    9000675
    Address
    7150 Koll Center Parkway
    City
    Pleasanton
    State
    CA
    Postal Code
    94566
    Country
    US

    Products

    Device Name Product Code
    System, Imaging, Pulsed Doppler, Ultrasonic IYN
    System, Imaging, Pulsed Echo, Ultrasonic IYO
    Transducer, Ultrasonic, Diagnostic ITX

    Proprietary Names

    Interson SiMPLi Series VPS Rhythm DLX Ultrasound Probe, Rebuilt VPS Rhythm DLX Ultrasound Probe

    Establishment Types

    Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer)