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510(k) Data Aggregation

    K Number
    K151852
    Date Cleared
    2015-11-10

    (126 days)

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

    PacEndo Sodium Hyprochlorite

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

    PacEndo™ Sodium Hypochlorite is intended to irrigate, cleanse, and debride root canal systems. It is also intended to provide irrigation during root canal instrumentation.

    Device Description

    PacEndo™ Sodium Hypochlorite is a Sodium Hypochlorite solution in water with surfactant to lower surface tension. The solution is root canal cleanser for use in endodontic procedures.

    AI/ML Overview

    The provided text describes the 510(k) premarket notification for PacEndo™ Sodium Hypochlorite. Here's an analysis of the acceptance criteria and study information:

    1. Table of Acceptance Criteria and Reported Device Performance

    The acceptance criteria are implicitly defined by the comparison to the predicate device in terms of performance characteristics. The document indicates that the subject device (PacEndo™ Sodium Hypochlorite) meets these criteria by demonstrating similar properties and, in one aspect, improved performance.

    Acceptance CriteriaReported Device Performance (PacEndo™ Sodium Hypochlorite)Predicate Device Performance (3% and 6% Sodium Hypochlorite with wetting agents marketed as Chlor-XTRA™ (K082470))
    Appearanceclear to light yellow liquidclear to light yellow liquid
    pH12.1112.02
    % Active Chlorine (w/w)4.6%5.3%
    Surface TensionLower surface tension compared to the predicate deviceHigher surface tension compared to the subject device (implied by the subject device's reported lower tension)

    2. Sample size used for the test set and the data provenance

    The document does not specify a distinct "test set" and its sample size in the context of clinical or large-scale comparative studies. The performance characteristics (Appearance, pH, % Active Chlorine (w/w), Surface Tension) are likely based on laboratory testing of batches of the product. No information is provided regarding the country of origin of the data or whether it was retrospective or prospective.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

    This information is not provided in the document. The type of device (sodium hypochlorite solution) does not typically involve expert interpretation for its core performance characteristics (pH, active chlorine, etc.).

    4. Adjudication method for the test set

    This information is not applicable and therefore not provided, as there is no indication of a test set requiring adjudication by multiple experts.

    5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

    There is no mention of an MRMC comparative effectiveness study, nor is AI assistance relevant to this type of device (a chemical solution).

    6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done

    This question is not applicable as the device is a chemical solution and does not involve algorithms or human-in-the-loop performance. The performance characteristics listed (appearance, pH, % active chlorine) are standalone measurements of the chemical product.

    7. The type of ground truth used

    The ground truth for the non-clinical tests (Appearance, pH, % Active Chlorine (w/w), Surface Tension) would be defined by standard chemical and physical measurement methods. For instance, pH meters, titration for active chlorine, and contact angle measurement for surface tension. There's no reliance on expert consensus, pathology, or outcomes data for these specific parameters.

    8. The sample size for the training set

    This information is not provided and is not applicable in the context of "training set" for an AI/algorithm-based device. If "training set" refers to the development and formulation of the chemical product, such details are not disclosed.

    9. How the ground truth for the training set was established

    As there is no "training set" in the context of AI/algorithm, this question is not applicable. For the development and quality control of the chemical product, the ground truth would be established through documented chemical and physical testing protocols and specifications.

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