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The Blease Frontline Genius Range, Anaesthesia Machines are intended for use in the hospital environment and locations not requiring portability. It may be used for the delivery of oxygen, air, and nitrous oxide in a controlled manner to various patient breathing circuits with or without the use of a mechanical ventilator, and may be used for the delivery of anaesthetic vapour by use of a dismountable vaporizer.

The device is intended for use only by a suitably qualified physician.

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This document is a 510(k) clearance letter from the FDA for an anesthesia machine (Blease Frontline Genius Range). It does not contain information about acceptance criteria or a study that proves the device meets specific acceptance criteria in the context of device performance as one would typically find for a new medical device that involves complex algorithms or AI.

Therefore, I cannot provide the requested table and information as it is not present in the provided text. The letter primarily confirms that the device is substantially equivalent to legally marketed predicate devices and outlines regulatory compliance.

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