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

    SLT CONTACT LASER SYSTEM ENDOPHOTOCOAGULATION

    K Number: K882441 · Decision Sep 26, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    26
    Registration Numbers
    27
    Same Product Code
    29
    Applicant Total
    51
    Review Days
    104

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    Basic Information

    Device Name
    SLT CONTACT LASER SYSTEM ENDOPHOTOCOAGULATION
    K Number
    K882441
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.4690
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Surgical Laser Technologies, Inc.
    Date Received
    June 14, 1988
    Decision Date
    September 26, 1988
    Product Code
    HQB
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HQB Photocoagulator And Accessories

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