BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇮🇳 India

    PLASTER CUTTING SCISSORS

    K Number: K892823 · Decision May 25, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    509
    Registration Numbers
    509
    Same Product Code
    17
    Applicant Total
    2
    Review Days
    44

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    Basic Information

    Device Name
    PLASTER CUTTING SCISSORS
    K Number
    K892823
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    The South India Surgical Co. Pvt. , Ltd.
    Date Received
    April 11, 1989
    Decision Date
    May 25, 1989
    Product Code
    LRW
    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
    LRW Scissors, General, Surgical

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    Other Clearances by The South India Surgical Co. Pvt. , Ltd.

    K Number Device Name
    K892820 FORCEPS, SURGICAL, GYNECOLOGICAL