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510(k) Data Aggregation

    K Number
    K040549
    Device Name
    COSMED PONY FX
    Manufacturer
    Date Cleared
    2004-09-28

    (210 days)

    Product Code
    Regulation Number
    868.1890
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    COSMED PONY FX

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

    The COSMED Pony FX pulmonary function testing system is a standalone and modular laboratory device for performing the basic lung function tests (Basic Spirometry: Forced Vital Capacity, Slow Vital Capacity, Maximum Voluntary Ventilation) and pulse oximetry.

    Device Description

    Not Found

    AI/ML Overview

    This document is a 510(k) clearance letter for the COSMED Pony FX, a pulmonary function testing system. It indicates that the device is substantially equivalent to legally marketed predicate devices.

    However, the provided text does not contain the information requested in your prompt regarding:

    • Acceptance criteria and reported device performance (Table 1)
    • Sample size and data provenance for the test set
    • Number and qualifications of experts for ground truth
    • Adjudication method
    • MRMC comparative effectiveness study results
    • Standalone algorithm performance
    • Type of ground truth used
    • Sample size and ground truth establishment for the training set

    The document primarily focuses on the regulatory clearance process, the device's indications for use (basic lung function tests and pulse oximetry), and regulatory compliance. It does not include details about specific performance studies or the methodology used to demonstrate substantial equivalence beyond a general statement of review.

    Therefore, I cannot fulfill your request for a detailed description of the acceptance criteria and study findings based on the provided text.

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