BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    EZ 502

    K Number: K844163 · Decision Mar 11, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    28
    Applicant Total
    2
    Review Days
    138

    Basic Information

    Device Name
    EZ 502
    K Number
    K844163
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4820
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    AEG POWER TOOL CORP.
    Date Received
    October 24, 1984
    Decision Date
    March 11, 1985
    Product Code
    KIJ
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

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    Other Clearances by AEG POWER TOOL CORP.

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