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

    E600B FOOTSWITCH

    K Number: K874794 · Decision Dec 14, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    2
    Applicant Total
    94
    Review Days
    21

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    Basic Information

    Device Name
    E600B FOOTSWITCH
    K Number
    K874794
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Valleylab, Inc.
    Date Received
    November 23, 1987
    Decision Date
    December 14, 1987
    Product Code
    BWA
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BWA Unit, Electrosurgical And Coagulation, With Accessories

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