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510(k) Data Aggregation

    K Number
    K220944
    Manufacturer
    Date Cleared
    2022-09-09

    (162 days)

    Product Code
    Regulation Number
    878.4040
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The PointCore Surgical Mask is intended to be worn to protect both the patient and healthcare personnel from transfer of microorganisms, body fluids and particulate material. These surgical masks are intended for use in infection control practices to reduce the potential exposure to blood and body fluids. This is a single use, disposable device provided nonsterile.

    Device Description

    The PointCore Surgical Mask is a surgical mask with ear loops and nose piece for fitting and securing the mask to the to the user's face. The ASTM Level of the subject device is ASTM Level 2. The finished size of the mask is 175mm x 95 mm. The masks are comprised of three layers: an outer polyethylene/polyester layer, a meltblown nonwoven filter layer, and an inner polypropylene layer. The mask also includes an adjustable nose strip and flat or round elastic ear loop. The nosepiece is manufactured from a reinforced plastic piece with a metal insert.

    AI/ML Overview

    The provided text is a 510(k) Summary for the PointCore Surgical Mask and contains information regarding performance testing against established standards, which serve as acceptance criteria. However, it does not describe a study involving an AI/Machine Learning device or human readers. The document is for a medical device (surgical mask), not an AI diagnostic/screening tool. Therefore, many of the requested categories are not applicable to this submission.

    Here's an analysis of the provided text against your requested criteria:

    The document describes the performance testing of a PointCore Surgical Mask, a physical medical device, not an AI or machine learning algorithm. Therefore, many of your requested items regarding AI/ML studies, human readers, and ground truth establishment for AI models are not applicable.

    However, I can extract the information relevant to the acceptance criteria and performance testing of the surgical mask:

    1. A table of acceptance criteria and the reported device performance

    The document references ASTM and other standards for performance testing. Here's a summary:

    Performance CharacteristicAcceptance Criteria (Standard Reference)Reported Device Performance (PointCore Surgical Mask)
    Fluid ResistanceASTM F1862Passed acceptance criteria of ASTM F1862
    Particle Filtration EfficiencyASTM F2299No specific numerical value reported, but implies meeting standard for ASTM Level 2 mask.
    Bacterial Filtration EfficiencyASTM F2101No specific numerical value reported, but implies meeting standard for ASTM Level 2 mask.
    Differential PressureMIL-M36945CNo specific numerical value reported, but implies meeting standard for ASTM Level 2 mask.
    Flammability16 CFR 1610No specific numerical value reported, but implies meeting standard.
    BiocompatibilityISO 10993No specific numerical value reported, but implies meeting standard.

    Note: For filtration efficiency, differential pressure, and flammability, the document states that the mask is "ASTM Level 2." While the exact numerical criteria for Level 2 are not explicitly listed in this document, meeting ASTM Level 2 for these characteristics implies meeting specific numerical thresholds defined by the ASTM standards.

    2. Sample sized used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective)

    This information is not provided in the document. The document only lists the standards used for testing (e.g., ASTM F1862) but does not detail the specific sample sizes used for each test or the provenance of the test materials.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience)

    This is not applicable. The device is a surgical mask, and its performance is evaluated against standardized physical and biological tests, not against expert medical interpretations or diagnoses.

    4. Adjudication method (e.g. 2+1, 3+1, none) for the test set

    This is not applicable. As explained above, the device is a surgical mask and its performance is determined by objective laboratory tests based on established standards, not by human adjudication of diagnostic outputs.

    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

    This is not applicable. No AI component is described for this device, and no MRMC study or human reader assistance is relevant to the performance of a surgical mask.

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

    This is not applicable. There is no algorithm or AI component in this device.

    7. The type of ground truth used (expert consensus, pathology, outcomes data, etc)

    The "ground truth" for a surgical mask's performance is established by objective measurements against internationally recognized standards (e.g., ASTM, MIL-M, CFR, ISO). For example:

    • Fluid Resistance: Measured by resistance to penetration by synthetic blood.
    • Filtration Efficiency: Measured by the ability to filter out specific sizes of particles or bacteria.
    • Differential Pressure: Measured by breathability.
    • Flammability: Measured by flame spread rate.
    • Biocompatibility: Measured by absence of cytotoxic, irritating, or sensitizing effects as per ISO 10993.

    8. The sample size for the training set

    This is not applicable. There is no AI/ML model for this device that would require a training set.

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

    This is not applicable. There is no AI/ML model for this device.

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