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510(k) Data Aggregation

    K Number
    K180408
    Date Cleared
    2018-04-13

    (58 days)

    Product Code
    Regulation Number
    892.1550
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The diagnostic ultrasound system (U60) is applicable for adults, pregnant women, pediatric patients' ultrasound evaluation in hospitals and clinics. It is intended for use in abdominal, obstetrics, gynecology, pediatric, small parts, urology, peripheral vascular, musculoskeletal (conventional and superficial), endovaginal and cardiac clinical applications, by or on the order of a physician or similarly qualified health care professional.

    Device Description

    The U60 is a portable Diagnostic Ultrasound System, which applies advanced technologies. Various image parameter adjustments, 15.0 inch LCD and diverse probes are configured to provide clear and stable images.

    AI/ML Overview

    The provided text is a 510(k) premarket notification for the Edan Instruments U60 Diagnostic Ultrasound System. This type of FDA submission aims to demonstrate "substantial equivalence" to a predicate device, rather than proving safety and effectiveness from scratch through extensive clinical trials for a new, revolutionary device.

    Therefore, the document does not contain detailed information about acceptance criteria and studies demonstrating that the device meets those acceptance criteria in the way one might expect for a novel AI/ML device or a device with new clinical indications. Instead, it focuses on demonstrating that the U60 is substantially equivalent to a predicate device (the U50 Diagnostic Ultrasound System) by showing similar design, intended use, indications for use, fundamental scientific technology, and performance, while complying with relevant safety standards.

    Here's a breakdown of what can and cannot be extracted from the document based on your request:

    Information Present in the Document:

    • 1. Table of Acceptance Criteria and Reported Device Performance:
      • The document presents a comparison table (within "9. Predicate Device Comparison") between the U60 (subject device) and the U50 (predicate device) across various parameters. This table effectively serves as the "acceptance criteria" for demonstrating substantial equivalence, where the acceptance criteria is generally "same" or "similar" to the predicate.
      • Table of Performance (Comparison to Predicate):
    ItemU60 R1.0 Ultrasound System (Edan Instruments) PerformanceU50 R2.2 Ultrasound System (Edan Instruments) PerformanceComparison Result
    Intended UseDiagnostic ultrasound imaging or fluid flow analysis of the human bodyDiagnostic ultrasound imaging or fluid flow analysis of the human bodySame
    Indications for UseApplicable for adults, pregnant women, pediatric patients' ultrasound evaluation in hospitals and clinics for abdominal, obstetrics, gynecology, pediatric, small parts, urology, peripheral vascular, musculoskeletal (conventional and superficial), endovaginal and cardiac clinical applications.Same as U60Same
    Safety StandardsIEC 60601-1, IEC 60601-1-2, IEC 60601-2-37, ISO 10993-1, -5, -10, AIUM, NEMA UD 2, UD3SameSame
    Patient Contact MaterialsComplies with ISO 10993Complies with ISO 10993Same
    Software life cycle processesComplies with IEC 62304Complies with IEC 62304Same
    Mode of OperationsContinuous operationContinuous operationSame
    General Imaging modeB-Mode, M-Mode, Color, PDI/DPDI, PW, CWB-Mode, M-Mode, Color, PDI/DPDI, PW, CWSame
    Measurements (B-Mode)Distance, Area, Volume, Ratio, Histogram, AngleSameSame
    Measurements (M-Mode)Distance, Time, Slope, Heart RateSameSame
    Measurements (D-Mode)Time, Heart Rate, Velocity, Acceleration, RI, PI, Auto (auto trace)SameSame
    Scanning methodElectronic convex, Electronic linear with slant scanningSameSame
    Cine loop1227 frames1227 framesSame
    Focus NumberMax=4Max=4Same
    Software PackagesAbdomen, obstetric, small parts, gynecology, cardiology, urology, vascular, Pediatrics.SameSame
    Principle of OperationApplying high voltage burst to Piezoelectric material in transducer and detect reflected echo to construct diagnostic imageSameSame
    Acoustic OutputTrack 3: MI, TIS, TIC, TIB (TI Range 0-6.0), Derated ISPTA: 720 W/cm² max, Mechanic Index ≤1.9 max or Derated ISPPA 190 W/cm² maxSameSame
    Transducer TypesConvex Array, Linear Array, Micro Convex Array, Phased ArraySameSame
    Transducer Frequency2.0-15.0 MHz2.0-15.0 MHzSame
    Primary Display15inch (1024*768)12.1inch (1024*768)Difference
    Dimensions/Weight220 mm (W) × 370 mm (L) × 350 mm (H), 8.1kg net weight330 mm (W) × 320 mm (L) × 220 mm (H), 7.8kg net weightDifference
    PrinterB/W video thermal printer, Color video thermal printer, Graph/text laser jet printerSameSame
    Storage MediaDVD, USB stickDVD, USB stickSame
    Temperature (Operating)0°C ~40°C5°C ~40°CDifference
    Temperature (Transport/Storage)-20~55°C-20~55°CSame
    Relative humidity (Operating)15% ~ 95%RH (no condensation)25% ~ 80%RH (no condensation)Difference
    Relative humidity (Transport/Storage)15% ~ 95%RH (no condensation)25% ~ 93%RH (no condensation)Difference
    Atmospheric pressure (Operating)860hPa ~1060hPa860hPa ~1060hPaSame
    Atmospheric pressure (Transport/Storage)700hPa ~1060hPa700hPa ~1060hPaSame
    Power RequirementsAC: 100-240V 50/60HzAC: 100-240V 50/60HzSame
    Operation SystemLinuxLinuxSame
    Safety ClassificationsClass I (Type BF, main unit: IPX0, probes: IPX7, footswitch: IP68, not suitable for use in flammable gas)SameSame
    Displayed depth20-320mm (Probe Dependent)20-320mm (Probe Dependent)Same
    Gray Scales256256Same
    Dynamic range150dB150dBSame
    TGC8 segments8 segmentsSame
    ZoomUp to 400%Up to 400%Same
    B-Mode Measurement AccuracyDepth/Distance: Max 324mm, Accuracy ≤±5%
    Area: Max 1126 cm², Accuracy ≤±10%
    Angle: 0-180°, Accuracy ≤±3%
    Ratio: Max 1.0, Accuracy
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