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Myflon Surgical Mask Level 3 is intended to be worn to protect both the patient and healthcare personnel from transfer of microorganisms, body fluids and particulate material. This face mask is 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 non-sterile.

The Myflon Surgical Mask Level 3 is blue in color, composed of three-layers, a flat-pleated type mask, utilizing ear loops for wearing. The Myflon Surgical Mask Level 3 materials consist of an outer cover (polypropylene spunbond, blue), middle filtration layer (polypropylene, melt-blown, white), and inner cover comfort/support layer web (polypropylene spunbond, white). Each mask has stretchable elastic laminate (Spunbond/elastic film/spunbond bond) ear loops to secure the mask over the user's mouth and nose and includes a polyethylene/ polypropylene coated wire nosepiece to provide a firm fit over the face and nose. This face mask is a single use, disposable device, provided non-sterile. This device is not made with natural rubber latex.

The provided text is a 510(k) summary for a surgical mask (Myflon Surgical Mask Level 3). It details the device, its intended use, and substantial equivalence to a predicate device based on non-clinical testing. It does not describe an AI/ML-driven medical device, an algorithm's performance, or any human-in-the-loop studies. Therefore, I cannot extract the information required to answer your specific questions related to AI/ML device acceptance criteria and study details.

The document explicitly states: "No clinical tests were performed." and describes the product as a physical surgical mask, not a software or AI device.

Therefore, I am unable to provide the requested information regarding:

1. A table of acceptance criteria and reported device performance for an AI/ML device.
2. Sample size used for the test set and data provenance.
3. Number of experts and their qualifications for establishing ground truth.
4. Adjudication method for the test set.
5. MRMC comparative effectiveness study and effect size.
6. Standalone (algorithm-only) performance.
7. Type of ground truth used.
8. Sample size for the training set.
9. How ground truth for the training set was established.

The acceptance criteria and performance data provided in the document pertain to the physical properties of the surgical mask, such as barrier testing (fluid resistance, particle filtration, bacterial filtration), flammability, differential pressure, and biocompatibility.

Here is the table of acceptance criteria and reported device performance for the surgical mask (as provided in the document), which is the only relevant information from the text:

Acceptance Criteria and Reported Device Performance (Myflon Surgical Mask Level 3)

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