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510(k) Data Aggregation

    K Number
    K073455
    Device Name
    E-VAC
    Date Cleared
    2008-03-25

    (106 days)

    Product Code
    Regulation Number
    878.4400
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The E-Vac Electrosurgery Suction Device removes smoke, odors, gases, particles, and fluids directly from the surgical site during electrosurgery procedures. The device is single-use and disposable.

    Device Description

    E-Vac Electrosurgery Suction Device

    AI/ML Overview

    This document is a marketing authorization letter for a medical device (E-Vac Electrosurgery Suction Device) based on a 510(k) premarket notification. It states that the device is substantially equivalent to legally marketed predicate devices.

    However, this document does not contain information about acceptance criteria or the results of a study proving the device meets acceptance criteria.

    The letter focuses on the regulatory clearance process and confirms that the device can be marketed. It does not provide details of performance testing or clinical studies.

    Therefore, I cannot provide the requested information based on the provided text. The document explicitly states: "We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices...". This means the device was found to be similar enough to a previously approved device, rather than undergoing extensive new performance studies to meet specific acceptance criteria.

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    K Number
    K061829
    Date Cleared
    2006-11-17

    (142 days)

    Product Code
    Regulation Number
    878.4400
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The BoVac Electrosurgery Suction Device removes smoke, odors, gases, particles, and fluids directly from the surgical site during electrosurgery procedures. The device is single-use and disposable.

    Device Description

    Not Found

    AI/ML Overview

    This document is a 510(k) clearance letter for the "BoVac Electrosurgery Suction Device." It indicates that the device has been found substantially equivalent to a predicate device, but it does not contain acceptance criteria or a study proving device performance against such criteria.

    The 510(k) clearance process focuses on demonstrating substantial equivalence to a legally marketed predicate device, rather than proving performance against pre-defined acceptance criteria through a dedicated study. This type of document typically does not include the detailed study information requested in the prompt.

    Therefore, I cannot provide the requested information based on the provided text.

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