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The VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500, when used with endoscopes, video endoscopes, camera heads, monitors and other ancillary equipment for endoscopic surgery, is intended to receive and process electronic signals transmitted from a video endoscope/camera head and output image signal to monitor.

The OLYMPUS OTV-S500 is a "universal platform" which offers compatibility with various endoscopes for different medical specialties and enables operation to meet the clinical needs in the fields of urology and gynecology. The Subject device is intended to be used in conjunction with ancillary equipment for endoscopic diagnosis, treatment and observation.

The OLYMPUS OTV-S500 consists of electrical circuit boards, electrical units (cooling fan, unit power supply, and control panel), harnesses between circuit boards, and optical components (lens and optical filter). A microprocessor is built into the OLYMPUS OTV-S500 which controls processing of observation images, user interface (front panel switch, indicator LEDs, warning buzzer etc.) and menu. These functions are implemented in the embedded software. Scopes including flexible videoscopes or fiberscopes and rigid videoscopes with camera heads and light source are directly connected to the Subject system. When connected, the endoscope (fiberscopes and rigid videoscope without camera head) acquires and displays images directly to the user or output onto a monitor when using a flexible endoscope or scope and camera head.

The Subject devices submitted for clearance include one (1) major component: the Video System Center (OLYMPUS OTV-S500); and two (2) auxiliary components: Foot Holder (MAJ-2552) for the OLYMPUS OTV-S500 that are shipped with the Video System Center, and an optional HDMI cable (MAJ-2551).

The provided document is a 510(k) Premarket Notification from the FDA for a medical device called "VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500 (OLYMPUS OTV-S500)". This document does not contain information about a study proving the device meets acceptance criteria for an AI/algorithm-driven device, as the device is an endoscope video system center, not an AI device.

Therefore, the requested information regarding acceptance criteria and performance study details for an AI/algorithm-driven medical device, including sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth types, training set details, and effect sizes, cannot be extracted from this document.

The document primarily focuses on non-clinical performance data to demonstrate substantial equivalence to a predicate device (OLYMPUS CV-170), covering aspects like:

• Performance Testing Bench: Field of View, Resolution, Image Noise and Dynamic Range, Brightness, Image Intensity Uniformity, Color Performance, Latency, and Contrast Enhancement.
• Electrical Safety/EMC Testing
• Software Validation/Cybersecurity

The summary explicitly states: "No clinical data were collected to support performance of the Subject device." This further confirms that the type of study you are asking about (often involving clinical performance, human readers, and AI output) was not conducted for this device.

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