BEUDAMED
    FDA Registration Active 🇺🇸 United States

    CATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION

    Reg #: 1222616 · FEI: 1000120916 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PRECISION OPTICS CORP.
    Registration Number
    1222616
    FEI Number
    1000120916
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    22 E Broadway
    City
    GARDNER
    State
    MA
    ZIP
    01440
    Country
    US

    Regulatory Submissions

    PMA Number
    P150026

    Owner / Operator

    Firm Name
    PRECISION OPTICS CORP.
    Operator Number
    9001379
    Address
    22 EAST BROADWAY, --
    City
    Gardner
    State
    MA
    Postal Code
    01440
    Country
    US
    Correspondent
    Sonny T Nguyen

    Products

    Device Name Product Code
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE

    Proprietary Names

    CATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)