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

    LEVTECH CLAMP APPLIER

    K Number: K874023 · Decision Nov 6, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    658
    Registration Numbers
    658
    Same Product Code
    72
    Applicant Total
    5
    Review Days
    35

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    Basic Information

    Device Name
    LEVTECH CLAMP APPLIER
    K Number
    K874023
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Levtech, Inc.
    Date Received
    October 2, 1987
    Decision Date
    November 6, 1987
    Product Code
    HTD
    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
    HTD Forceps

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