Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K974493
    Device Name
    FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES
    Date Cleared
    1998-03-31

    (123 days)

    Product Code
    Regulation Number
    876.1500
    Why did this record match?
    Applicant Name (Manufacturer) :

    FIEGERT-ENDOTECH MEDIZINTECHNIK GMBH

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Provide illumination to, and allow visual observation and/or surgical manipulation of body cavities, hollow organs and canals in the Gastrointestinal tract.
    Device Description
    Fiegert Endotech Flexible Fiberoptic Endoscopes; Fiegert Endotech Flexible Video-Endoscopes
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1