LogoFDA 510(k) Search
Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K992045
    Device Name
    ELECTROSURGICAL ELECTRODE FAMILY
    Manufacturer
    GENESIS MEDICAL, INC.
    Date Cleared
    2000-01-27

    (224 days)

    Product Code
    GEI
    Regulation Number
    878.4400
    Why did this record match?
    Applicant Name (Manufacturer) :

    GENESIS MEDICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Indicated for coagulation of tissue These devices are intended for use by qualified medical personnel trained in the use of electrosurgery.
    Device Description
    Not Found
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1