Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K173803
    Device Name
    Omnican fine
    Date Cleared
    2018-06-11

    (178 days)

    Product Code
    Regulation Number
    880.5570
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Omnican fine is intended for use with compatible needle-based injection systems for subcutaneous injection of fluid drug products.

    Device Description

    The Omnican fine is a pen needle device that is a sterile, individually packaged, single use, hypodermic single lumen needle; intended for use with compatible needle-based injection systems for subcutaneous injection of fluid drug products. Omnican fine is a double-ended needle consisting of a tri-beveled tip, hollow steel cannula, and needle hub packaged in a hard plastic sealed container. Specific versions contain an inner needle shield. The Omnican fine provides a fluid path from a drug container to subcutaneous tissue.

    AI/ML Overview

    The provided text describes a 510(k) premarket notification for a medical device, specifically a hypodermic single lumen needle called "Omnican fine." The purpose of a 510(k) submission is to demonstrate substantial equivalence to a legally marketed predicate device, not necessarily to prove absolute safety and effectiveness through extensive clinical trials. Therefore, the "study" referred to will be a collection of non-clinical performance tests and comparisons.

    Here's a breakdown of the acceptance criteria and the "study" details based on the document:

    1. Table of Acceptance Criteria and the Reported Device Performance:

    The document outlines acceptance criteria indirectly through the "Summary of nonclinical performance tests" and lists the intended performance of the "Proposed Device Omnican fine."

    Feature/TestAcceptance Criteria (Predicate/Omnican Fine)Reported Device Performance (Omnican fine)
    Functional Performance
    Measurement of needle tube length: Injector end6.15 +0.5/-0.3 mm6.15 +0.5/-0.3 mm
    Measurement of needle tube length: Patient End12 +1.1/-0.8 mm (for 12mm size)
    8 +1.1/-0.8 mm (for 8mm size)
    6 +1.1/-0.8 mm (for 6mm size)
    4 + 1.25/-0.0 mm (for 4mm size)12 +1.1/-0.8 mm
    8 +1.1/-0.8 mm
    6 +1.1/-0.8 mm
    4 + 1.25/-0.0 mm
    Dislocation of measuring point at patient end≤ 1.1 mm (for 12mm needle)
    ≤ 0.9 mm (for 8mm needle)
    ≤ 0.7 mm (for 6mm needle)
    ≤ 0.6 mm (for 4mm needle)Met criteria (implied by "Omnican fine met all established acceptance criteria")
    Bond between needle hub and needle tubeWithstand a 22 N force applied axially for 5 seconds.Met criteria (implied by "Omnican fine met all established acceptance criteria")
    Unscrewing torque of the needle
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1