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

    PARA-VENT

    K Number: K791463 · Decision Sep 17, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    94
    Registration Numbers
    94
    Same Product Code
    18
    Applicant Total
    1
    Review Days
    42

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    Basic Information

    Device Name
    PARA-VENT
    K Number
    K791463
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.5320
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Cameron Medical Corp.
    Date Received
    August 6, 1979
    Decision Date
    September 17, 1979
    Product Code
    BTC
    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
    BTC Bag, Reservoir

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