RHYNOSTAT H-12 & V-22

RHYNOSTAT H-12 & V-22 is an FDA 510(k)-cleared medical device (K852349) manufactured by Remesta Medical Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 2, 1985. Regulation: 8.