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

    MINUTEMAN CO2 MICROSURGICAL LASER GYN

    K Number: K843515 · Decision Feb 4, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    47
    Applicant Total
    5
    Review Days
    152

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    Basic Information

    Device Name
    MINUTEMAN CO2 MICROSURGICAL LASER GYN
    K Number
    K843515
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4550
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    American Surgical Laser, Inc.
    Date Received
    September 5, 1984
    Decision Date
    February 4, 1985
    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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    Other Clearances by American Surgical Laser, Inc.

    K Number Device Name
    K843519 MINUTEMAN CO2 MICROSURG LASER GEN SURG
    K843518 MINUTEMAN C02 MICROSURG LASER PODIATRY
    K843517 MINUTEMAN CO2 MICROSURG LASER DERMATOL-
    K843514 MINUTEMAN CO2 MICROSURGICAL LASER OTO