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510(k) Data Aggregation

    K Number
    K023973
    Manufacturer
    Date Cleared
    2003-02-27

    (87 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 AutoMed 3200 ambulatory infusion pump with integrated administration set is intended for general infusion use. Routes of infusion include intravenous, percutaneous, subcutaneous, inter-arterial and epidural, and into intra-operative (soft tissue / body cavity) sites. The AutoMed 3200 infusion pump is also intended for patient-controlled infusion using the integrated bolus button. General infusion uses include continuous infusion of a local anesthetic near a nerve for regional anesthesia and pain management for pre-operative, perioperative and postoperative surgery.

    Device Description

    The AutoMed 3200 infusion pump with integrated administration set and drug reservoir is a rotary peristaltic pump. Associated dedicated administration set, AM 330, and accessories are part of the overall system. The system is suitable for use as an ambulatory device and is intended for use in the hospital, home environment or alternative care sites.

    AI/ML Overview

    This document describes the AutoMed 3200 infusion pump, a rotary peristaltic pump intended for general infusion use, including patient-controlled infusion. The device is significantly similar to several predicate devices. The information provided does not include acceptance criteria or a study that proves the device meets specific performance criteria. The document is primarily a 510(k) premarket notification summary and an FDA clearance letter for the device, focusing on its intended use and substantial equivalence to existing products.

    Therefore, I cannot provide the requested information regarding acceptance criteria and studies demonstrating device performance based on the input text. The text does not contain:

    1. A table of acceptance criteria and reported device performance.
    2. Sample sizes or data provenance for a test set.
    3. Details about experts used for ground truth or adjudication methods.
    4. Information on multi-reader multi-case (MRMC) studies or effect sizes.
    5. A standalone algorithm performance study.
    6. The type of ground truth used (e.g., pathology, outcomes data).
    7. Sample size for a training set.
    8. How ground truth was established for a training set.
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