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510(k) Data Aggregation

    K Number
    K243783
    Date Cleared
    2025-03-12

    (93 days)

    Product Code
    Regulation Number
    890.3900
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Applicant Name (Manufacturer) :

    Shenzhen Zuowei Technology Co., Ltd.

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

    Walking rehabilitation training electric wheelchair is to provide indoor mobility, including stand-up feature, to persons limited to a seating position that are capable of operating a powered wheelchair.

    Device Description

    Walking rehabilitation training electric wheelchair (ZW518)

    AI/ML Overview

    This FDA 510(k) clearance letter for the "Walking rehabilitation training electric wheelchair (ZW518)" does not contain any information about acceptance criteria or a study proving that the device meets such criteria.

    The document is a regulatory clearance letter, confirming that the FDA has determined the device is substantially equivalent to legally marketed predicate devices. It discusses regulatory compliance, labeling, quality systems, and other administrative requirements for marketing the device.

    Therefore, I cannot provide the requested information, including:

    1. A table of acceptance criteria and reported device performance.
    2. Sample size and data provenance for the test set.
    3. Number and qualifications of experts for ground truth.
    4. Adjudication method.
    5. MRMC comparative effectiveness study details.
    6. Standalone performance details.
    7. Type of ground truth used.
    8. Sample size for the training set.
    9. Method for establishing training set ground truth.

    This document pertains to the regulatory pathway for market clearance, not the detailed technical and performance validation studies.

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