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510(k) Data Aggregation

    K Number
    K091414
    Manufacturer
    Date Cleared
    2009-10-21

    (161 days)

    Product Code
    Regulation Number
    870.1130
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The BioCare vTrust 701DH NIBP monitor is a compact, battery-powered monitor which measures noninvasive blood pressure (systolic and mean arterial pressure) and pulse rate based on the principle of plethysmography (oscillometric on inflation). This equipment is intended for use only by qualified medical providers in conjunction with established medical protocols. It is not intended for use in an MRU environment, or in an air transport environment.

    Device Description

    The BioCare vTrust 701DH NIBP monitor is a compact, battery-powered monitor which measures noninvasive blood pressure (systolic, diastolic and mean arterial pressure) and pulse rate based on the principle of plethysmography (oscillometric on inflation). The oscillometric method detects volume displacements within the artery and senses pressure variations within the blood pressure cuff during inflation. The measurement is more quickly and with less patient discomfort than with monitors which measure NIBP during cuff deflation. Cycle time function enables you to pre-set measurement intervals. User can set alarm limits by selectable for high or low range.

    AI/ML Overview

    1. Table of Acceptance Criteria and Reported Device Performance:

    ClausePerformance CharacteristicsMax. permissible error or acceptance criteriaReported Device Performance (Max. deviation)Passed/Failed
    4.2.1Storage conditions: [23°F(-5°C)] for 24 hrs; [122°F(50°C)] for 24 hrs; RH: 90% (noncondensing)≤± 3 mmHg (±0.4 kPa) ≤± 4 mmHg for in use-3.4 mmHgPassed
    4.2.2Operating conditions: Temp: 50°F (10°C)104°F(40℃); RH: 1590% (noncondensing); Bar. 105kPa80kPa (790mmHg600mmHg)≤± 3 mmHg (±0.4 kPa) ≤±4 mmHg for in use± 3 mmHgPassed
    4.2.3Vibration and shock: ISTA-standard drop and vibration test IEC 60601-1, sections 21.5 & 21.6ISTA-1A: 14,200 vibratory impacts; drop test-10 drops; before and after transportation test within ±5 mmHg of the average reading.no visible damage; SD ≤8 mmHgPassed
    4.2.4.1Voltage range: Battery-powered devices-indication of battery conditionRed light: low battery; Blue light: batteries are charging; Green light: fully charged25 mmHg/secmmHg/sec
    4.3.2Electrical safety:IEC 60601-1, 1988; Amendment 1, 1991; & Amendment 2, 1995.N/APassed
    4.4.3.1.ARange: 0 mmHg to at least 260 mmHg by visual inspectionNIBP pressure calibration0~300 mmHgPassed
    4.4.3.2.AResolution: 1 mmHg by visual inspectionNIBP pressure calibration1 mmHgPassed
    4.4.3.3.AAccuracy of pressure measurement: Ambient temp 10°C~40°C; RH: 15%~90%; Pressure stages: 50, 100, 150, 200, 250, 300 mmHg≤±3 mmHg (±0.4 kPa) or 2% of the reading; ≤±4 mmHg for in use±3 mmHgPassed
    4.4.3.4.ARepeatability Cuff-Link simulator test for stability and reproduction of performance Adult: SYS120/DIA80/MAP90 mmHg, 80 BPM Neo: SYS80/DIA50/MAP62 mmHg, 120 BPMAverage difference ≤± 5 mmHg5 mmHgPassed
    4.4.3.6.ALeakage: Ambient temp 15°C25°C; RH: 2085%; Pressure stages: 50, 100, 150, 200, 250 mmHg, wait at least 60 s before reading the values.≤6 mmHg/min1.2 mmHg/minPassed
    4.4.4.BPressure transducer accuracy: Ambient temp 10℃~40℃; RH: 15%~90%; Pressure stages: 50, 100, 150, 200, 250, 300 mmHg≤±3 mmHg (±0.4 kPa) or 2% of the reading; ≤±4 mmHg for in use±3 mmHgPassed
    4.4.5.BOverall system efficacy-clinical testing (auscultatory method as the reference Std.) no fewer than 85 subjects with a minimum of 255(=3*85) observationsFor systolic and diastolic: mean≤±5 mmHg; SD ≤8 mmHgMean: Sys/Dia 3.4/-4.5; SD: Sys/Dia 5.23/4.64 mmHgPassed
    4.5.1Inflation source: pressure~300mmHg≤10sNIBP pressure calibration: inflate at 5 mmHg/sec; Speed test: Inflation > 5 mmHg/secN/APassed
    4.5.4.3.BAutomated valves-Release rate: rapid exhaust with fully-opened valve260mmHg → 15mmHg ≤10 sec or 150mmHg → 5mmHg ≤5 secdeflate at 25 mmHg/secPassed
    IEC 60601-2-30Automatic cycling function 1. In long term automatic mode (normal condition) Adult 120/80(90)[SYS/DIA(MAP)]--long term Neonate 80/50(62)[SYS/DIA(MAP)]--long term 2. In long term automatic mode (single fault condition) 3. In short term automatic mode (stat mode)1. deflated time ≥30 sec; mean≤± 5 mmHg; 2. deflated time ≤30 sec; release cuff pressure to below 15mmHg(adult)/ 5mmHg(neo.); 3. deflated time≥2sec. after each determination1. average for adults 34 sec / for neonates 42 sec; -4mmHg; 2.
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