POLY/PLATINUM WIRE PISTON

POLY/PLATINUM WIRE PISTON is an FDA 510(k)-cleared medical device (K945105) manufactured by Micromed Development Corp.. 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 May 13, 1996. Regulation: 8.