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510(k) Data Aggregation

    K Number
    K033963
    Date Cleared
    2004-04-15

    (115 days)

    Product Code
    Regulation Number
    870.1220
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    EP DEFLECTABLE CATHETERS

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

    The EP Deflectable Catheters are designed for one time single patient use for temporary use in electrophysiology studies. Models can be use in conjunction with EPMedSystems' EP Workmate.

    Device Description

    EP Deflectable Catheters

    AI/ML Overview

    I am sorry, but based on the provided document, there is no information available regarding acceptance criteria or a study that proves the device meets those criteria.

    The document is a 510(k) clearance letter from the FDA for the "EP Deflectable Catheter." This letter primarily addresses the substantial equivalence of the device to legally marketed predicate devices, allowing it to proceed to market. It does not contain details about the specific performance metrics, clinical studies, or acceptance criteria that would typically be required to answer your request.

    Therefore, I cannot provide:

    1. A table of acceptance criteria and the reported device performance.
    2. Sample size used for the test set and the data provenance.
    3. Number of experts used to establish the ground truth for the test set and their qualifications.
    4. Adjudication method.
    5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, or its effect size.
    6. If a standalone performance study was done.
    7. The type of ground truth used.
    8. The sample size for the training set.
    9. How the ground truth for the training set was established.

    To obtain this kind of information, you would typically need to consult the original 510(k) submission, scientific publications about the device, or contact EPMedSystems directly.

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