CAP PORP, CAP TORP

CAP PORP, CAP TORP is an FDA 510(k)-cleared medical device (K000256) manufactured by Gyrus Ent LLC. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 10, 2000. Regulation: 8.