BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    1.9 FRENCH LITHOTRIPTER ELECTRODE, MODIFICATION

    K Number: K914514 · Decision Jan 6, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    36
    Registration Numbers
    36
    Same Product Code
    60
    Applicant Total
    55
    Review Days
    89

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    Basic Information

    Device Name
    1.9 FRENCH LITHOTRIPTER ELECTRODE, MODIFICATION
    K Number
    K914514
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.4480
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Northgate Technologies, Inc.
    Date Received
    October 9, 1991
    Decision Date
    January 6, 1992
    Product Code
    FFK
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FFK Lithotriptor, Electro-Hydraulic

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