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

    FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA

    K Number: K862444 · Decision Sep 25, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    47
    Applicant Total
    12
    Review Days
    91

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    Basic Information

    Device Name
    FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA
    K Number
    K862444
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4550
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Laser Media
    Date Received
    June 26, 1986
    Decision Date
    September 25, 1986
    Product Code
    HHR
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HHR Laser, Surgical, Gynecologic

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