Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K152840
    Manufacturer
    Date Cleared
    2015-12-02

    (64 days)

    Product Code
    Regulation Number
    870.1250
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Lantern Delivery Microcatheter

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

    Lantern Delivery Microcatheter is intended to assist in the delivery of diagnostic agents, such as contrast media, and therapeutic devices, such as occlusion coils, to the peripheral and neuro vasculature.

    Device Description

    Lantern Delivery Microcatheter is a single lumen intravascular catheter designed to aid physician in accessing distal vasculature. When used in conjunction with a guide catheter and guide wire, Lantern provides access to the target site. Once in place it provides a reinforcing conduit for other intravascular devices.

    AI/ML Overview

    This document describes the Lantern™ Delivery Microcatheter and its substantial equivalence to a predicate device. The information provided focuses on the non-clinical data, specifically biocompatibility and bench-top testing, to demonstrate its safety and effectiveness.

    Here's a breakdown of the requested information based on the provided text:

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

    TestAcceptance CriteriaReported Device Performance/Results
    In vitro Cytotoxicity (MEM Elution)Sample extracts must yield cell lysis grade $\le$ 2Grade: 1 (slight) - Met
    Sensitization (Magnusson-Kligman Method)Test Group shall yield Grade 10% in 3 or more animalsNon-toxic - Met
    Material Mediated Rabbit PyrogenSample extracts must not cause a total rise in body temperature of $\ge$ 0.5° CNon-pyrogenic - Met
    Hemolysis – Indirect ContactSample extracts must be nonhemolytic ($\le$ 2% hemolytic index)Non-hemolytic - Met
    Complement ActivationThe concentrations of C3a and SC5b-9 in the test samples are statistically similar to the predicate control and statistically lower than the positive control for all exposure timesNo greater biological response than corresponding control - Met
    Thrombosis (Dog Thrombogenicity)Device must be non-thrombogenic after 4 hours in vivo when compared to control deviceNon-thrombogenic - Met
    Bench-top Testing (various tests)All predetermined requirements (specific criteria not detailed for each individual test in the document)All established acceptance criteria were met. All testing met specification. - Met
    Pyrogenicity (LAL validation)
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1