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510(k) Data Aggregation

    K Number
    K961292
    Date Cleared
    1996-11-06

    (216 days)

    Product Code
    Regulation Number
    870.5800
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The proposed device is to be used to improve the return circulation of body fluid that has pooled in one or more of a patient's extremities. This treatment reduces debilitating pain, swelling, ulceration, and risk of dermatological impact, infection, and amputation.

    Device Description

    This is an electromechanical pneumatic device that employs a compressor and precision timer, regulator, and gage to sequentially inflate a sleeve appliance that fits over the patient's extremity. The device is approximately 8"W x 6.75"H x 5.5"D and weighs less than 15 lbs.

    AI/ML Overview

    The prompt asks to describe the acceptance criteria and the study that proves the device meets them, based on the provided text. However, the provided text describes a "Wright Linear Pump" which is a sequential compression pump, not an AI/ML powered medical device. Therefore, many of the requested fields are not applicable to the given text.

    Here's an analysis based on the provided information, noting where sections are not applicable:

    1. Table of Acceptance Criteria and Reported Device Performance

    Acceptance Criteria (Explicit or Implied)Reported Device Performance
    Functional / Performance:
    Produces sequential compressionProduces sequential compression
    Max pressure
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