Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K964447
    Manufacturer
    Date Cleared
    1997-04-16

    (161 days)

    Product Code
    Regulation Number
    880.5970
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Peripherally inserted central venous (PICC) and midline catheters placed for venous access or prolonged intravenous therapy.

    Device Description

    Peripherally inserted central venous (PICC) and midline catheters placed for venous access or prolonged intravenous therapy. Method of insertion is through an introducer sheath. The optimal catheter tip location for the PICC catheter is in the superior vena cava of the heart. The recommended tip location for the midline catheter is below the shoulder, at the level of the axilla. The products will be available in single and dual lumen configurations; with and without a flushable guidewire; and as sterile individual units or in insertion kits containing the components used for insertion of the device.

    AI/ML Overview

    This document is a Summary of Safety and Effectiveness Information for medical devices (PICC and Midline Catheters). It does not describe an AI/ML powered device, therefore, the information requested in your prompt (e.g., acceptance criteria for an algorithm, sample sizes for test/training sets, expert consensus for ground truth, MRMC studies) are not applicable to the provided text.

    The document focuses on the safety and effectiveness of a physical medical device (catheter) based on engineering and biocompatibility tests, not on the performance of a software algorithm.

    Here's a breakdown of what the document does provide in relation to traditional medical device testing:

    1. A table of acceptance criteria and the reported device performance:

    The document provides a table of tests and their conclusions, which implicitly refer to meeting acceptance criteria for each physical test. The column "Conclusion" being "Passed" indicates that the device met the pre-defined acceptance criteria for that specific test.

    TestConclusion
    Flow ratePassed
    Tensile strength of bodyPassed
    Tensile strength of catheter to hubPassed
    Catheter stiffnessPassed
    Catheter elongationPassed
    Leakage at hub jointPassed
    Burst pressure (positive pressure)Passed
    Catheter collapse (negative pressure)Passed
    Biocompatibility per ISO 10993Passed
    SterilizationPassed

    The remaining points (2-9) are not applicable to this physical device submission. This document details the physical and biological performance of a catheter, not an AI system.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1