Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K946168
    Manufacturer
    Date Cleared
    1996-03-21

    (458 days)

    Product Code
    Regulation Number
    880.5725
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The intended use for the IVAC enteral administration sets is to provide nutrition to patients who have an impaired ability to orally ingest their food. The pumping segment or cassette of the enteral administration set interacts with the pumping mechanism of the infusion pump to regulate fluid flow at the desired rate.

    Device Description

    The IVAC enteral administration sets (Series 28XXX, 28XX6, 52XXX, 52XX6, 59XXX, 59XX6) incorporate standard IVAC set components and materials. The sets include an enteral adapter and. with some configurations, a pre-attached bag which holds the enteral formula during delivery. The enteral adapter is incompatible with standard ANSI IV set luers which prevents the user from accidentally attaching the enteral adapter to an intravenous set. The infusion pumps regulate fluid flow at the desired rate.

    AI/ML Overview

    The provided text is a 510(k) summary for medical devices, specifically enteral administration sets and infusion pumps. It describes the devices, their intended use, and technological characteristics compared to predicate devices to establish substantial equivalence.

    However, the document does not contain any information regarding clinical studies, acceptance criteria for device performance based on measurable outcomes, or any of the detailed data provenance, expert ground truth establishment, or multi-reader studies that your request asks for.

    The text focuses on demonstrating "substantial equivalence" based on manufacturing methods, components, and primary functions, which is common for 510(k) submissions for devices that are not high-risk and are similar to already marketed devices. It does not include performance metrics or clinical trial data in the way an AI/ML device submission would.

    Therefore, I cannot populate the table or answer the specific questions about acceptance criteria, study details, sample sizes, ground truth, or MRMC studies, as this information is not present in the provided text.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1