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510(k) Data Aggregation

    K Number
    K954220
    Device Name
    EUB-8000
    Date Cleared
    1997-05-07

    (604 days)

    Product Code
    Regulation Number
    892.1550
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    EUB-8000

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Not Found

    Device Description

    The Hitachi EUB-8000 Ultrasound Electronic Scanner is a Track 3 diagnostic ultrasound system capable of the following operating modes: B, M, Pulsed Doppler, Color Flow, and Continuous Wave Doppler. Probes available with the EUB-8000 are intended for the following general clinical uses: Abdominal, Cardiac, Intra-operative , Fetal, Pediatric, Small Organ, Peripheral Vascular, Biopsy, Transvaginal, Transvaginal, and Neonatal Cephalic. The EUB-8000 utilizes digital front-end electronics for detection of echo signals.

    AI/ML Overview

    The provided text is a summary of safety and effectiveness for the Hitachi EUB-8000 Ultrasound Electronic Scanner. It describes the device, its intended uses, and its compliance with safety standards regarding acoustic output and general electrical safety.

    However, the provided text does not contain any information regarding acceptance criteria, device performance studies, sample sizes, ground truth establishment, expert qualifications, or adjudication methods. Therefore, I cannot generate the requested table or answer the specific questions about the study that proves the device meets acceptance criteria.

    The document focuses on:

    • Device Description: What the device is and its capabilities (B, M, Pulsed Doppler, Color Flow, CW Doppler modes).
    • Intended Use: The clinical applications for which the probes are designed (Abdominal, Cardiac, Intra-operative, Fetal, Pediatric, Small Organ, Peripheral Vascular, Biopsy, Transvaginal, Transvaginal, and Neonatal Cephalic).
    • Safety Compliance: Adherence to NEMA UD-3 for acoustic output and IEC 601-1 for general electrical safety.

    To answer your questions, additional documentation detailing performance studies and clinical evaluation would be required.

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