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

    CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY

    K Number: K912833 · Decision Sep 23, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    97
    Registration Numbers
    97
    Same Product Code
    76
    Applicant Total
    18
    Review Days
    89

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    Basic Information

    Device Name
    CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY
    K Number
    K912833
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1110
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Camino Laboratories, Inc.
    Date Received
    June 26, 1991
    Decision Date
    September 23, 1991
    Product Code
    DSK
    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
    DSK Computer, Blood-Pressure

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