MEDILAS H RFID LASER FIBER

MEDILAS H RFID LASER FIBER is an FDA 510(k)-cleared medical device (K121938) manufactured by Dornier Medtech America, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 31, 2012. Regulation: 8.