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The 3S Safety Syringe with/without Needle is a sterile, single-use, disposable and non-reusable, manual retractable safety syringe intended for injection of fluids into the body, while reducing the risk of sharps injuries and the potential for syringe reuse.

The 3S Safety Syringe with/without Needle is an integrated needle and piston syringe with an innovative anti-needle-stick mechanism. The design incorporates the ideal features desired in a safety syringe. No special techniques are required to use the safety mechanism. The mechanism allows clear visualization of the injection site at all times. The mechanism clearly shows the needle is contained within the syringe barrel. After standard techniques for injection, the plunger is withdrawn, snapped off and used syringe is discarded into a sharps container per regulatory provision.

This document is primarily a 510(k) summary for a medical device (3S Safety Syringe). It focuses on establishing substantial equivalence to a predicate device rather than detailing extensive clinical study results as one might find in a PMA or a more comprehensive clinical trial report.

Therefore, many of your requested items, particularly those related to AI algorithm performance, sample sizes for test/training sets in an AI context, expert ground truth establishment for AI, MRMC studies, and standalone AI performance, are not applicable to this document as it describes a physical safety syringe, not an AI/software device.

However, I can extract the acceptance criteria and performance related to the physical device.

1. Table of Acceptance Criteria and Reported Device Performance

For the 3S Safety Syringe, the acceptance criteria are generally based on conformity to international standards and regulations. The "reported device performance" is essentially a statement of this conformity.

Note: This table reflects the information present in the provided document, which is a 510(k) summary. It asserts equivalence to established standards rather than providing raw performance data or a detailed study report.

Information Not Applicable or Not Provided in the Document:

The following information is not contained within the provided 510(k) summary, as it pertains to AI/software device studies or detailed clinical trial breakdowns not typically required for a Class II physical medical device 510(k) submission focused on substantial equivalence.

2. Sample size used for the test set and the data provenance: Not applicable for this type of physical device submission. Performance is assessed against engineering standards, not a data test set in the AI sense.
3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable. Ground truth for a physical syringe's performance is established by engineering testing against standards (e.g., fluid leakage, plunger force, sterility, biocompatibility), not by expert consensus on data interpretation.
4. Adjudication method for the test set: Not applicable.
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: Not applicable, as this is not an AI device.
6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done: Not applicable.
7. The type of ground truth used: For a physical device like a syringe, "ground truth" refers to the objective physical and chemical properties and performance characteristics measured against established international standards (ISO, biological safety) and regulatory requirements (CFR). It's not an "expert consensus" or "pathology" in the diagnostic sense.
8. The sample size for the training set: Not applicable, as there is no AI training set.
9. How the ground truth for the training set was established: Not applicable.

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