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

    SL-100 ND:YAG LASER FOR UROLOGIC SURGERY

    K Number: K871516 · Decision Jul 9, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    59
    Applicant Total
    7
    Review Days
    80

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    Basic Information

    Device Name
    SL-100 ND:YAG LASER FOR UROLOGIC SURGERY
    K Number
    K871516
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Medical Energy, Inc.
    Date Received
    April 20, 1987
    Decision Date
    July 9, 1987
    Product Code
    LNK
    Advisory Committee
    General, Plastic Surgery
    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
    LNK Laser For Gastro-Urology Use

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    Other Clearances by Medical Energy, Inc.

    K Number Device Name
    K041419 LIGHTFORCE LF 20/30 980NM SURGICAL DIODE LASER SYSTEM
    K871512 SL-100 ND:YAG LASER FOR GYNECOLOGY USE
    K871511 SL-100 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS
    K871513 SL-100 ND:YAG LASER FOR PALLIATION OF GASTRO. MALI
    K871514 SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID
    K871515 SL-100 ND:YAG LASER FOR GASTROINTESTINAL BLEEDING