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

    PERCUDISC PLDD DELIVERY SYSTEM/PROCEDURE KIT

    K Number: K920673 · Decision Aug 13, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    478
    Registration Numbers
    480
    Same Product Code
    2867
    Applicant Total
    2
    Review Days
    181

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    Basic Information

    Device Name
    PERCUDISC PLDD DELIVERY SYSTEM/PROCEDURE KIT
    K Number
    K920673
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Percudisc, Inc.
    Date Received
    February 14, 1992
    Decision Date
    August 13, 1992
    Product Code
    GEX
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GEX Powered Laser Surgical Instrument

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    Other Clearances by Percudisc, Inc.

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