ARTAIRA Arterial Compression Device (AACD01)

ARTAIRA Arterial Compression Device (AACD01) is an FDA 510(k)-cleared medical device (K240499) manufactured by Airos Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 10, 2024. Regulation: 8.