BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    MODEL CBX EPILATOR

    K Number: K884079 · Decision Oct 4, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24
    Same Product Code
    42
    Applicant Total
    13
    Review Days
    7

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    Basic Information

    Device Name
    MODEL CBX EPILATOR
    K Number
    K884079
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.5350
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    R. A. Fischer Co. Corp.
    Date Received
    September 27, 1988
    Decision Date
    October 4, 1988
    Product Code
    KCW
    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
    KCW Epilator, High Frequency, Needle-Type

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