BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MABIS BRAND AND MABIS CUSTOMERS PRIVATE LABEL BRAND

    K Number: K942072 · Decision May 10, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    428
    Registration Numbers
    428
    Same Product Code
    1216
    Applicant Total
    2
    Review Days
    376

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    Basic Information

    Device Name
    MABIS BRAND AND MABIS CUSTOMERS PRIVATE LABEL BRAND
    K Number
    K942072
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1130
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Mabis Healthcare, Inc.
    Date Received
    April 29, 1994
    Decision Date
    May 10, 1995
    Product Code
    DXN
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXN System, Measurement, Blood-Pressure, Non-Invasive

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    Other Clearances by Mabis Healthcare, Inc.

    K Number Device Name
    K990506 MABIS NB-02 ULTRASONIC NEBULIZER