Midas Flowmeter; eAVS

Midas Flowmeter; eAVS is an FDA 510(k)-cleared medical device (K241465) manufactured by Parker Hannifin Corporation. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 18, 2024. Regulation: 8.