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

    ELEKIBAN MAGNETO-THERAPEUTIC DEVICE

    K Number: K850172 · Decision Apr 16, 1985
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    90

    Basic Information

    Device Name
    ELEKIBAN MAGNETO-THERAPEUTIC DEVICE
    K Number
    K850172
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    MNS, LTD.
    Date Received
    January 16, 1985
    Decision Date
    April 16, 1985
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N