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DC-90/DC-90S/DC-900/DC-95/DC-95S/DC-88/DC-80A/DC-80A Exp/DC-80A Pro/DC-80A Pro/DC-8X/DC-80/DC-80/DC-80/DC-80/DC-81/ DC-82 Diagnostic Ultrasound System is applicable for adults, pregnant women, pediatric patients and neonates. It is intended for use in fetal, abdominal, pediatic, small organ(breast, thyroid, testes), neonatal and adult cephalic, transrectal, trans-vaginal, musculo-skeletal(conventional, superficial), adult and pediative cardiac, peripheral vessel and urology exams.

DC-90/DC-90S/DC-90Q/DC-95/DC-95S/DC-88/DC-88S/DC-80A/DC-80A Exp/DC-80A Pro/DC-8X/DC-8Q/DC-81/DC-82 Diagnostic Ultrasound System is a general purpose, mobile, software controlled, ultrasound diagnostic system. Its function is to acquire and display ultrasound images in B-mode, M-mode, PW-mode, CW mode, Color-mode, Color M-mode, Power/Dirpower mode, TDI mode, THI, iScape, Biopsy Guidance, 3D/4D mode, Elastography, Contrast imaging or the combined mode (i.e. B/M-Mode).This system is a Track 3 device that employs an array of probes that include linear array, convex array and phased array.

The provided text describes the regulatory clearance for the DC-90/DC-90S/DC-90Q/DC-95/DC-95S/DC-88/DC-88S/DC-80A/DC-80A Exp/DC-80A Pro/DC-8X/DC-8Q/DC-81/DC-82 Diagnostic Ultrasound System. However, it does not contain specific acceptance criteria, detailed study results, or performance metrics for an AI model.

The document primarily focuses on demonstrating substantial equivalence to predicate devices through technical specifications, intended uses, and compliance with various safety and performance standards for an ultrasound system, not an AI component. It states "Clinical Tests: Not Applicable." indicating that a clinical study to prove the device meets acceptance criteria via performance metrics for an AI system was not performed or deemed necessary for this 510(k) submission.

Therefore, I cannot populate the requested tables and information based on the provided text, as the information is not present. The document is about the FDA clearance of an ultrasound system, not an AI software/device that would typically have specific performance acceptance criteria demonstrated through a clinical study with detailed results, ground truth, and expert evaluation.

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