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510(k) Data Aggregation

    K Number
    K963490
    Date Cleared
    1996-11-12

    (70 days)

    Product Code
    Regulation Number
    880.6760
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    These devices are Universal Gait Belt, Wheelchair Belt, Foam Limb Restraint, Double Buckle Limb Restraint, Comfort Safety Belt, Comfort Slider Belt, Universal Roll Belt and belt style restraints used to restrain patients in a wheelchair or bed. The devices are labeled for prescription use and are not intended for lay use.

    Device Description

    These devices are made of polyester, cotton, nylon and polyethelen configured into either a mesh or weave substrate. Each device utilizes straps for securing (tie) the patient in place.

    AI/ML Overview

    This 510(k) summary (K96-3490) is for patient restraint devices, not a digital health device or AI-powered medical device. Therefore, the requested information about acceptance criteria, study details, ground truth, and AI performance metrics is not applicable to this submission.

    The document describes physical patient restraint devices (Gait Belts, Wheelchair Belts, Limb Restraints, Safety Belts, Roll Belts). The summary states: "These devices have been commercially distributed for over for years and have not been associated with an MDR type complaint." This statement serves as the de facto "proof" that the device meets safety and effectiveness criteria for substantial equivalence, implying a history of safe use rather than a formal clinical study with performance metrics.

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