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

    VENTI-MONITOR MODEL 101

    K Number: K812041 · Decision Sep 25, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    55
    Registration Numbers
    55
    Same Product Code
    77
    Applicant Total
    14
    Review Days
    66

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    Basic Information

    Device Name
    VENTI-MONITOR MODEL 101
    K Number
    K812041
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.2600
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Medix Medical Electronics (U.S.A.), Inc.
    Date Received
    July 21, 1981
    Decision Date
    September 25, 1981
    Product Code
    CAP
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

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    Other Clearances by Medix Medical Electronics (U.S.A.), Inc.

    K Number Device Name
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    K853393 INSULIN PUMP INSUMAT 229
    K852433 INFUSAFE 205 CATOLOG NO. 205.000
    K813562 SYRINGE DRIVER 209
    K812039 SPIROMETER 210/211
    K812045 INFANT APNEA MONITOR MODEL 100
    K812040 OXYGEN MONITOR 140/141
    K812046 TIDAL VOLUME MONITOR 150
    K812044 RESPIRATION RATE MONITOR 120/121
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