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510(k) Data Aggregation

    K Number
    K051474
    Date Cleared
    2005-07-01

    (28 days)

    Product Code
    Regulation Number
    880.5725
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SYMBIOS DISPOSABLE INFUSION PUMP KIT

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

    The Symbios Disposable Infusion Pump Kit is a disposable, self-contained infusion system utilizing an inflatable elastomeric reservoir to mechanically provide percutaneous infusion of prescribed solutions at a pre-set rate for post-operative pain management.
    The Disposable Infusion Pump is a disposable, self-contained infusion system utilizing an inflatable elastomeric reservoir to mechanically provide percutaneous infusion of prescribed solutions at a proset rate for post-operative pain management.

    Device Description

    The Symbios Disposable Infusion Pump Kit is a convenience kit that includes the components necessary to provide temporary infusion of a liquid into a patient. The components of the system are an elastomeric pump, a catheter needle/introducer, an infusion catheter and a bandage. The pump is a disposable, self-contained, infusion system utilizing an inflatable elastomeric reservoir to mechanically pressurize a fluid and drive it through tubing to a small restrictor to provide infusion at a pre-set rate.
    The device is provided empty and no specific drug references are made in the labeling. The device is not intended for delivery of blood, blood products, lipids or fat emulsions.

    AI/ML Overview

    I am sorry, but the provided text does not contain the information required to describe the acceptance criteria and the study that proves the device meets the acceptance criteria. The document is a 510(k) premarket notification for a "Disposable Infusion Pump Kit," which includes information about its classification, description, and intended use, along with FDA correspondence confirming substantial equivalence to predicate devices.

    However, it does not include:

    • A table of acceptance criteria and reported device performance.
    • Details about a study (like sample size, data provenance, ground truth establishment, expert involvement, or adjudication methods).
    • Information about MRMC comparative effectiveness studies or standalone algorithm performance.

    The document primarily focuses on regulatory approval based on substantial equivalence, rather than a detailed performance study with quantifiable acceptance criteria.

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