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

    LME BLOOD PRESSURE MONITOR

    K Number: K832017 · Decision Oct 31, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    97
    Registration Numbers
    97
    Same Product Code
    76
    Applicant Total
    38
    Review Days
    130

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    Basic Information

    Device Name
    LME BLOOD PRESSURE MONITOR
    K Number
    K832017
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1110
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Litton Medical Electronics
    Date Received
    June 23, 1983
    Decision Date
    October 31, 1983
    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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    Other Clearances by Litton Medical Electronics

    K Number Device Name
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    K840523 SERVOMED PULSE AMPLIFIER MODULE-206-
    K840524 SERVOMED BASIC BEDSIDE UNIT SMV 110TP
    K840209 SERVOMED MEDIVISION SCOPE SMV-235
    K840832 SERVOMED OXCARDIORE SPIROGRAPH 324/111
    K840521 SERVOMED DIGITAL DISPLAY MODULE
    K832250 SERVOMED BASIC BEDSIDE UNIT SMA 102-
    K832998 2-CHANNEL RECORDER
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