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

    MILEX KEGEL PERINEAL EXERCISER

    K Number: K862410 · Decision Jul 31, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28
    Same Product Code
    64
    Applicant Total
    8
    Review Days
    36

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    Basic Information

    Device Name
    MILEX KEGEL PERINEAL EXERCISER
    K Number
    K862410
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1425
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Milex Products, Inc.
    Date Received
    June 25, 1986
    Decision Date
    July 31, 1986
    Product Code
    HIR
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HIR Perineometer

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