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

    RODEL ELECTRODERM PADS

    K Number: K802658 · Decision Dec 30, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    56
    Registration Numbers
    56
    Same Product Code
    68
    Applicant Total
    2
    Review Days
    67

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    Basic Information

    Device Name
    RODEL ELECTRODERM PADS
    K Number
    K802658
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1275
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Rodel Products Corp.
    Date Received
    October 24, 1980
    Decision Date
    December 30, 1980
    Product Code
    GYB
    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
    GYB Media, Electroconductive

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    Other Clearances by Rodel Products Corp.

    K Number Device Name
    K812299 ELECTRO-SNAP