AirSeal iFS System; AirSeal dV Solution

AirSeal iFS System; AirSeal dV Solution is an FDA 510(k)-cleared medical device (K230239) manufactured by Conmed Corporation. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 2023. Regulation: 8.