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

    MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC

    K Number: K902976 · Decision Sep 7, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22
    Same Product Code
    57
    Applicant Total
    6
    Review Days
    63

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    Basic Information

    Device Name
    MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC
    K Number
    K902976
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1330
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Medical Consultants Intl. , Ltd.
    Date Received
    July 6, 1990
    Decision Date
    September 7, 1990
    Product Code
    GZL
    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
    GZL Electrode, Depth

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    Other Clearances by Medical Consultants Intl. , Ltd.

    K Number Device Name
    K904264 MODEL SW-103 SOLITANS STIMULATOR
    K900731 MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)
    K903654 LISS CRANIAL STIMULATOR MODEL SBL202-B
    K894515 LISS CRANIAL STIMULATOR MODEL SBL201-M
    K896226 LISS BODY STIMULATOR MODEL SBL501-M