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510(k) Data Aggregation

    K Number
    K233789
    Manufacturer
    Date Cleared
    2024-04-10

    (134 days)

    Product Code
    Regulation Number
    878.5070
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    8Q10 Surclear Smoke Plume Evacuation System

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

    The Surnic Surclear Smoke Plume Evacuation System with accessories is intended to remove smoke created in surgical procedures at the surgical site.

    Device Description

    The Surclear 8010 have been designed with a high suction, high flow rate vacuum motor. The ultra-quiet motor is used to draw the surgical smoke from the surgical site through the vacuum tubing and into the Surclear 8010 filter 8QF1 where the surgical smoke is processed by a series of filters. A single disposable filter is used to simplify the installation and removal during filter changes. The filter is completely enclosed to protect the healthcare personnel from potential contamination during filter changes. One 8QF1 filter contains four different stages within to capture the smoke plume.

    AI/ML Overview

    The provided text describes the acceptance criteria and the results of non-clinical tests for the 8Q10 Surclear Smoke Plume Evacuation System. It does not contain information about a study proving the device meets the acceptance criteria in the context of an AI/human-in-the-loop performance evaluation, which is typically found in submissions for AI-powered devices.

    The information provided pertains to the safety and functional performance of a medical device (a smoke plume evacuation system), not an AI/software as a medical device (SaMD). Therefore, many of the requested criteria (like sample size for test set, data provenance, number of experts, MRMC studies, etc.) are not applicable or not provided in this document.

    However, I can extract and present the information that is available:


    Acceptance Criteria and Reported Device Performance for the 8Q10 Surclear Smoke Plume Evacuation System

    This document describes the non-clinical testing conducted to demonstrate the safety and functionality of the 8Q10 Surclear Smoke Plume Evacuation System.

    1. Table of Acceptance Criteria and Reported Device Performance

    Title of TestPurpose of TestAcceptance CriteriaResults
    Electrical Safety TestingEvaluate Electrical SafetyFulfil the requirement of IEC 60601-1:2012+2020 as applicablePassed
    Electromagnetic CompatibilityEvaluate Electromagnetic CompatibilityFulfil the requirements of IEC 60601-1-2:2014+2020 as applicablePassed
    Software ValidationEvaluate Device SoftwareAll test cases shall pass or deviations explained as to why it is acceptablePassed
    Flow Rate TestingEvaluate flow rate against design requirementThe flow rates at each flow mode are within the defined tolerances.Passed
    Plume Evacuation EvaluateEvaluate System for evacuation of plume generated by medical devicesFulfil the requirements of ISO 16571:2014 as applicablePassed

    Further Technological Characteristics and Comparison to Predicate Device:

    CharacteristicSubject Device (K233789)Predicate Device (K131402)Discussion
    Indications for UseRemove smoke created in surgical procedures at the surgical site.Remove and filter smoke and aerosols from a surgical site produced during electrosurgical and laser procedures.Similar
    Static Motor Suction25.69 kPa25.69 kPaSame
    Flow rates (Max)25 cfm (707 lpm) @7/8(22mm) tubing30 cfm (839 lpm) @7/8(22mm) tubingSimilar, (cfm) 25vs30 is due to different manufacturers' understanding of the maximum flow limit required in actual applications.
    Suction control level10 Level10 LevelThere are 10 control levels of suction rate from 10% to 100%.
    Suction blockage warningYesYesAn occlusion warning safety feature alerts the operator when an occlusion has occurred.
    Foot controlYesYesThe operator can foot-control the suction of the device to turn on or off.
    Filter life indicationYesYesCounter indicates filter status and lifetime.
    Filter performance99.99% efficiency at 0.1-to-0.2-micron particle size with a filter life of up to 40 hours.99.99% efficiency at 0.1-to-0.2-micron particle size with a filter life of up to 35 hours.Same filter efficiency, larger filters can increase application time from 35 to 40 hrs.
    Power Supply100-120VAC, 50/60Hz, 9A max; 220-240VAC, 50/60Hz, 4.5A max100/240VAC, 50/60Hz; 220/240 VACSame

    Information Not Found in the Provided Text:

    The following specific requested information is not available in the given document, as it pertains to AI/SaMD performance studies, which is not the subject of this 510(k) submission:

    1. Sample size used for the test set and the data provenance: Not applicable/not provided for a hardware device's functional testing. The tests are against specific engineering and safety standards.
    2. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable. Ground truth for a smoke evacuator's performance is based on physical measurements and compliance with engineering standards.
    3. Adjudication method for the test set: Not applicable.
    4. If a multi reader multi case (MRMC) comparative effectiveness study was done: Not applicable.
    5. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done: Not applicable.
    6. The type of ground truth used: For this device, ground truth is based on established international (IEC, ISO) and industry standards for electrical safety, electromagnetic compatibility, software validation, flow rates, and plume evacuation.
    7. The sample size for the training set: Not applicable (not an AI/ML device).
    8. How the ground truth for the training set was established: Not applicable (not an AI/ML device).
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