Search Filters

Search Results

Found 27 results

510(k) Data Aggregation

    K Number
    K240127
    Device Name
    PlumeSafe X5 Smoke Management System
    Manufacturer
    CONMED Corporation
    Date Cleared
    2024-08-05

    (201 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The CONMED PlumeSafe® X5™ Smoke Management System is designed to remove and filter smoke and aerosols from a surgical site produced during electrosurgical and laser procedures.
    Device Description
    The PlumeSafe® X5™ Smoke Management System is a portable, stand-alone, capital unit, that when paired with a reusable filter and disposable accessories makes up a Smoke Management System. The smoke unit is accompanied by a reusable filter and is available in two different configurations, a 22mm or 25mm size. Each filter is designed to capture components of surgical smoke and return clean air to the environment and can connect to different accessories which include pencils, adapters, fluid traps, and tube sets. Each filter is a seff-contained device that is completely enclosed to protect health care personnels from potential contamination during filter changes. Each filter is comprised of filtration (gross particulate pre-filter, Ultra-Low Penetration Air (ULPA), coconutbased carbon, impregnated alumina, and carbon dust capture media) that produce capture efficiency ratings equal to or better than 99.999% for particles ranging in size from 0.01μm to 0.2μm. PlumeSafe® X5™ is comprised of a vacuum motor, aluminum, steel, and plastic components combined with sound reducing insulation. The vacuum motor is used to draw the surgical site, through an accessory, and into the PlumeSafe® X5™ filter. The PlumeSafe® X5™ Smoke Management System provides multiple modes (open, laparoscopic, and pencil) and settings to adjust the flow to the clinical need.
    Ask a Question
    K Number
    K233789
    Device Name
    8Q10 Surclear Smoke Plume Evacuation System
    Manufacturer
    Surnic Corporation
    Date Cleared
    2024-04-10

    (134 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    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.
    Ask a Question
    K Number
    K230547
    Device Name
    PlumePen Elite Surgical Smoke Evacuation Pencils, PlumePen Pro Surgical Smoke Evacuation Pencil, PlumePen Ultra Surgical Smoke Evacuation Pencils, PenAdapt Electrosurgical Pencil Adapter, SnapEvac Electrosurgical Pencil Adapter
    Manufacturer
    ConMed Corporation
    Date Cleared
    2023-04-27

    (58 days)

    Product Code
    GEI, FYD, REG
    Regulation Number
    878.4400
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SnapEvac and PenAdapt is an aspiration sheath that fits over an electrosurgical pencil body and leaves the tip or blade exposed. This device is considered an accessory to an electrosurgical unit (ESU). SnapEvac and PenAdapt removes surgical smoke during surgical procedures that use ESU for cutting and cauterizing. This device is used in conjunction with a suction (vacuum) source. Contraindications: This device should not be used for microsurgery. The PlumePen® Elite, PlumePen® Ultra, and PlumePen® Pro is designed for general electrosurgical applications, including cutting and coagulation, and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. The pencil enables the operator to remotely conduct an electrosurgical current from the output connector of an electrosurgical unit to the operative site for the desired surgical effect. Indicated for use to remove smoke plume from the surgical site and to remotely conduct an electrosurgical current from the output connector of an electrosurgical unit to the target tissue for the desired surgical effect.
    Device Description
    The smoke evacuation devices that are the subject of this 510(k) are PlumePen Surgical Smoke Evacuation Pencils (Elite, Pro and Ultra), PenAdapt Electrosurgical Pencil Adapters and Electrosurgical Pencil Adapters. By interfacing with an effective smoke evacuation unit, these devices function as part of the system to remove smoke particles from the point of surgical activity during procedures that use an electrosurgical unit (ESU) for cutting and cauterizing. PlumePen Smoke Evacuation Pencils: The PlumePen® Elite, Pro, and Ultra family of devices are sterile, single use electrosurgical hand pieces featuring an integrated smoke evacuation channel. The devices, when connected to an electrosurgical generator and smoke evacuation system are designed to remove smoke plume generated during the use of the pencil for electrosurgical procedures. PenAdapt and SnapEvac Electrosurgical Pencil Adapters: PenAdapt and SnapEvac are sterile, single use pencil adapters which fit over standard electrosurgical pencils while keeping the blade exposed. They enable the capture and removal of smoke generated during the use of the pencil, in procedures that require cutting and cauterization, when connected to an effective smoke evacuation system.
    Ask a Question
    K Number
    K213068
    Device Name
    Medline Smoke Evacuation Shroud
    Manufacturer
    Medline Industries, Inc.
    Date Cleared
    2022-01-03

    (102 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Medline's Smoke Evacuation Shroud is a single use, sterile product. Its intended use is as an electrosurgical accessory to attach to a standard cautery pencil. The shroud removes surgical procedures. The product is used inside the sterile field.
    Device Description
    Medline's Smoke Evacuation Shroud is a single use, sterile product.
    Ask a Question
    K Number
    K202944
    Device Name
    NEBULAE SRS Laparoscopic Surgical Smoke Removal System
    Manufacturer
    Northgate Technologies Inc.
    Date Cleared
    2021-03-25

    (176 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    To remove airborne particles generated by tissue combustion during laparoscopic surgery, via filtration of gaseous media contained within the distended pneumoperitoneum in order to improve visualization. NEBULAE® SRS may be used in any laparoscopic surgery, as appropriate.
    Device Description
    This 510(k) submission for the NEBULAE® SRS Laparoscopic Surgical Smoke Removal System (henceforth referred to as NEBULAE® SRS) covers the following product codes: • NEBULAE® SRS Pump (7-700-00) • NEBULAE® SRS CO₂ Gas Filtration Tubing Sets (7-510-57) The NEBULAE® SRS is intended to recirculate CO2 gas in the pneumoperitoneum whilst removing surgical smoke during laparoscopic procedures. The system consists of two parts: a Pump and dedicated singleuse, sterile Tubing Sets. The NEBULAE® SRS Pump is a microprocessor driven, mains-powered device containing a DC motor. The single-use, disposable Tubing Set consists of an integrated cartridge, containing a diaphragm pump, an in-line ultra-low particulate air (ULPA) with activated carbon filter, fluid trap(s), 10 feet of DEHP-free PVC tubing and two connectors for connecting the tubing to the trocars. The NEBULAE® SRS Pump's DC motor drives the pump head in the Tubing Set's cartridge to create the flow of CO2 gas from the patient's pneumoperitoneum, through the fluid trap(s) and filter before re-entering the patient. The NEBULAE® SRS Pump can be positioned on a level surface (e.g. a surgical trolley in the operating room) or fixed to a vertical IV pole using a dedicated bracket, which is available as an accessory (See VOLUME 011 for further information). The re-circulating CO2 gas can also be warmed by the addition of an in-line gas warmer, also available as an optional accessory.
    Ask a Question
    K Number
    K200250
    Device Name
    Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF Sensor
    Manufacturer
    Megadyne Medical Products, Inc.
    Date Cleared
    2020-06-26

    (144 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Megadyne Smoke Evacuator with accessories is intended to remove smoke created in surgical procedures at the surgical site.
    Device Description
    The Megadyne Smoke Evacuator is designed to provide smoke evacuation in open and Laparoscopic procedures for the removal of surgical smoke. Using a scroll pump and 4 stages of filtration, the Megadyne Smoke Evacuator is designed to evacuate surgical smoke both quietly and effectively. An intuitive front panel design allows users to customize both the rate of suction FLOW and the length of RUN TIME after the active electrode is deactivated. Push button selections for OPEN, LAP (laparoscopic), and MANUAL modes are also clearly marked and easily accessible. The Megadyne smoke evacuator provides evacuation of smoke plume via a smoke evacuation device and tubing (e.g. E-Z Clear Smoke Evacuation Electrosurgical Pencil under K141587 on February 18, 2015) connected to the face of the Filter.
    Ask a Question
    K Number
    K192035
    Device Name
    EvaQMax Smoke Evacuation System
    Manufacturer
    Bio Protech, Inc.
    Date Cleared
    2019-08-29

    (30 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    To remove and filter smoke and aerosols from a surgical site produced during electrosurgical and laser procedures.
    Device Description
    Not Found
    Ask a Question
    K Number
    K191328
    Device Name
    Megadyne Foot Switch
    Manufacturer
    Megadyne Medical Products, Inc.
    Date Cleared
    2019-07-26

    (71 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Megadyne Foot Switch is an accessory that is interface with compatible smoke evacuation systems to control on/off inputs for manual operation.
    Device Description
    The Megadyne Foot Switch is used with a compatible smoke evaluation system to control on/off inputs for manual operation.
    Ask a Question
    K Number
    K182224
    Device Name
    SafeAir Smoke Evacuator compact
    Manufacturer
    LiNA Medical APS
    Date Cleared
    2019-02-07

    (175 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    SafeAir Smoke Evacuator compact is designed to remove and filter smoke generated during electrosurgical and laser procedures.
    Device Description
    SafeAir Smoke Evacuator compact is a device with a vacuum pump that aspirates the surgical smoke produced during cauterization. The main purpose of smoke evacuation systems is to remove surgical smoke plume as close as possible to the surgical site. The component of the system ensuring that this is achieved is a diathermy pencil with integrated smoke evacuation function or a click-on tubing set connected to a surgical smoke evacuator. SafeAir Smoke Evacuator compact is designed for use in the hospital/clinic environment. It is built around a vacuum pump with a replaceable filter at the entry point. A specially designed pump control is centrally placed in the machine. The SafeAir Smoke Evacuator compact is designed with a pump with different activation functions; manual activation on the front panel, footswitch activation through diathermy pencil with smoke evacuation tubing. Synchronization is possible with most of the electrosurgical units.
    Ask a Question
    K Number
    K173108
    Device Name
    Smoklean
    Manufacturer
    Sejong Medical Co., Ltd.
    Date Cleared
    2018-05-18

    (231 days)

    Product Code
    FYD
    Regulation Number
    878.5070
    Why did this record match?
    Search-Everything :

    Matched: '878.5070'

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Smoklean is a passive smoke evacuation system which removes particles from surgical smoke generated in laparoscopic procedures while maintaining a clear field of vision.
    Device Description
    During the laparoscopic surgery, the smoke generated by the electrocautery dims the surgeon's vision, affecting the operation and causing the smoke to have a negative effect on the surgeon. It is used in connection with a laparoscopic trocar body or a single port used to expand the surgical site during laparoscopic surgery. This product filters smoke generated when the tissue is cauterized through the laparoscopic trocar body and a single port. The connecting part of the Trocar body or single port is 4.25 * 5.04mm in diameter. The device is consisted of 35cm tubing, a body with filters and an adaptor.
    Ask a Question

    Page 1 of 3