BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇵🇰 Pakistan

    PERCUSSION HAMMER

    K Number: K891571 · Decision Mar 31, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    10
    Applicant Total
    1
    Review Days
    11

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    Basic Information

    Device Name
    PERCUSSION HAMMER
    K Number
    K891571
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    882.1700
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Sandal Surgico
    Date Received
    March 20, 1989
    Decision Date
    March 31, 1989
    Product Code
    GWZ
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GWZ Percussor

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