BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

    VENTIPRESS 24 AND 14 PRESSURE VENTILATOR

    K Number: K893950 · Decision Aug 3, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    95
    Registration Numbers
    95
    Same Product Code
    152
    Applicant Total
    1
    Review Days
    63

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    Basic Information

    Device Name
    VENTIPRESS 24 AND 14 PRESSURE VENTILATOR
    K Number
    K893950
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5650
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Ventipress OY
    Date Received
    June 1, 1989
    Decision Date
    August 3, 1989
    Product Code
    IRP
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IRP Massager, Powered Inflatable Tube

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