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

    DERMATRON IONTOPHORESIS DEVICE

    K Number: K780310 · Decision Jul 31, 1978
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    4
    Review Days
    160

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    Basic Information

    Device Name
    DERMATRON IONTOPHORESIS DEVICE
    K Number
    K780310
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Motion Control, Inc.
    Date Received
    February 21, 1978
    Decision Date
    July 31, 1978
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Other Clearances by Motion Control, Inc.

    K Number Device Name
    K872040 PHORESOR II (TM), MODEL PM700
    K862236 MYOLAB II, MODEL ML-200
    K802642 UTAH ARTIFICAL ARM