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510(k) Data Aggregation

    K Number
    K013838
    Date Cleared
    2002-01-16

    (58 days)

    Product Code
    Regulation Number
    874.4760
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    KSEA CLEARVISION LENS IRRIGATION SYSTEM

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

    The KSEA Clearvision® is a lens irrigation system for cleaning the lens and maintaining clear visualization without removing the scope from the surgical site during sinus surgery.

    Device Description

    The KSEA Clearvision® is a microprocessor-controlled pump device. The device provides irrigation to clean the objective lens of scope, and removes residual solution on the lens. It is used in conjunction with an irrigation sheath.

    AI/ML Overview

    This 510(k) summary does not contain the information required to answer your request.

    Here's why:

    • Acceptance Criteria and Device Performance: The document does not describe specific performance-based acceptance criteria (e.g., a certain flow rate, cleaning effectiveness percentage) or present data from a study demonstrating the device meets such criteria. Instead, it focuses on substantial equivalence to a predicate device based on features and intended use.
    • Study Details (Sample Size, Provenance, Ground Truth, Training Set): There is no mention of a study involving a test set, training set, or the establishment of ground truth. The submission is a regulatory comparison against a predicate device, not a performance study.
    • Expert Review/Adjudication: Since no performance study (like a clinical trial or algorithm evaluation) is presented, there's no information about experts used for ground truth, their qualifications, or adjudication methods.
    • MRMC or Standalone Studies: The document does not discuss multi-reader multi-case comparative effectiveness studies or standalone performance studies. The KSEA Clearvision is a physical pump device, not an AI or imaging-based diagnostic tool that would typically undergo such studies.

    In summary, this 510(k) pertains to a medical device's regulatory clearance based on substantial equivalence, rather than a detailed performance study with acceptance criteria.

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