BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    SURGICAL INSTRUMENT

    K Number: K833542 · Decision Nov 28, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    444
    Registration Numbers
    445
    Same Product Code
    103
    Applicant Total
    8
    Review Days
    62

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    Basic Information

    Device Name
    SURGICAL INSTRUMENT
    K Number
    K833542
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Hirata Sangyo Co. USA, Inc.
    Date Received
    September 27, 1983
    Decision Date
    November 28, 1983
    Product Code
    GEN
    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
    GEN Forceps, General & Plastic Surgery

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