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510(k) Data Aggregation

    K Number
    K962871
    Date Cleared
    1996-10-23

    (92 days)

    Product Code
    Regulation Number
    868.5470
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    ODS1 - HOOD DRIVER

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

    Hyperbaric chambers are used for treating the indications as currently listed by the Undersea Hyperbaric & Medical Association for hyperbaric oxygen therapy.

    Device Description

    The Model ODS1 - Hood Driver is intended for use with monoplace hyperbaric chambers. It is normally used to permit the patient to breath oxygen while the chamber is pressurized on air. However, it can be used to supply the patient with any physiologically appropriate gas which may or may not be the same as the gas used to pressurize the chamber. The ODSI circuit is designed to supply a steady flow of breathing gas to the breathing apparatus used in the chamber. The breathing apparatus can be either a "Sea-Long" hood or a free-flow mask arrangement.

    AI/ML Overview

    The provided text is a 510(k) summary for a hyperbaric chamber breathing station (ODS1 Hood Driver). It does not contain information about acceptance criteria, device performance, sample sizes, data provenance, expert qualifications, adjudication methods, multi-reader multi-case studies, standalone performance, ground truth types, or training set details that would be found in a study proving a device meets acceptance criteria.

    This document describes the device's function, its intended use, and compares it to a similar, already legally marketed device (Lifeforce Hyperbaric Chamber System) to demonstrate substantial equivalence. This is a regulatory submission, not a clinical study report.

    Therefore, I cannot provide the requested information from the given text as it is not present.

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