BEUDAMED
    FDA Registration Active 🇺🇸 United States

    DERM 941 High Frequency Desiccator

    Reg #: 3007593903 · FEI: 3007593903 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Apyx Medical Corporation
    Registration Number
    3007593903
    FEI Number
    3007593903
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    5115 Ulmerton Rd
    City
    Clearwater
    State
    FL
    ZIP
    33760
    Country
    US

    Regulatory Submissions

    510(k) Number
    K161134

    Owner / Operator

    Firm Name
    Apyx Medical Corporation
    Operator Number
    9910100
    Address
    5115 ULMERTON ROAD, --
    City
    Clearwater
    State
    FL
    Postal Code
    33760
    Country
    US
    Correspondent
    Angela Huber

    Products

    Device Name Product Code
    Electrosurgical, Cutting & Coagulation & Accessories GEI

    Proprietary Names

    DERM 941 High Frequency Desiccator Bantam PRO Electrosurgical Generator DERM 942 High Frequency Desiccator

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)