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

    PFISTER-SCHWARTZ STONE RETRIEVER

    K Number: K771302 · Decision Aug 2, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    27
    Registration Numbers
    27
    Same Product Code
    18
    Applicant Total
    41
    Review Days
    18

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    Basic Information

    Device Name
    PFISTER-SCHWARTZ STONE RETRIEVER
    K Number
    K771302
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.4680
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    V. Mueller O.V. Baxter Healthcare Corp.
    Date Received
    July 15, 1977
    Decision Date
    August 2, 1977
    Product Code
    FGO
    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
    FGO Dislodger, Stone, Flexible

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