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

    DISPOSA-LITE LARYNGOSCOPE BLADE

    K Number: K832984 · Decision Oct 28, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    315
    Registration Numbers
    315
    Same Product Code
    63
    Applicant Total
    2
    Review Days
    56

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    Basic Information

    Device Name
    DISPOSA-LITE LARYNGOSCOPE BLADE
    K Number
    K832984
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.5540
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Michael S. Upsher
    Date Received
    September 2, 1983
    Decision Date
    October 28, 1983
    Product Code
    CCW
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CCW Laryngoscope, Rigid

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    Other Clearances by Michael S. Upsher

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