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

    SERVOMED MEDIVISION SCOPE SMV-235

    K Number: K840209 · Decision Sep 20, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    38
    Registration Numbers
    38
    Same Product Code
    77
    Applicant Total
    38
    Review Days
    245

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    Basic Information

    Device Name
    SERVOMED MEDIVISION SCOPE SMV-235
    K Number
    K840209
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2450
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Litton Medical Electronics
    Date Received
    January 19, 1984
    Decision Date
    September 20, 1984
    Product Code
    DXJ
    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
    DXJ Display, Cathode-Ray Tube, Medical

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    Other Clearances by Litton Medical Electronics

    K Number Device Name
    K840522 RECOMED BLOOD-FLOW METER H236-052-02
    K840899 SERVOMED ARRHYCOMP CENTRAL MONITOR SYS
    K840439 RECOMED CARDIAC OUTPUT METER 236067-
    K840523 SERVOMED PULSE AMPLIFIER MODULE-206-
    K840524 SERVOMED BASIC BEDSIDE UNIT SMV 110TP
    K840832 SERVOMED OXCARDIORE SPIROGRAPH 324/111
    K840521 SERVOMED DIGITAL DISPLAY MODULE
    K832250 SERVOMED BASIC BEDSIDE UNIT SMA 102-
    K832998 2-CHANNEL RECORDER
    K834600 RECOMB ECG PREAMPLIFIER/206 069 03
    Search all 38 clearances from Litton Medical Electronics →