MICROPROBE LASER AND ENDOSCOPY SYSTEM, MODEL E2

MICROPROBE LASER AND ENDOSCOPY SYSTEM, MODEL E2 is an FDA 510(k)-cleared medical device (K042918) manufactured by Endooptiks, 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 November 21, 2004. Regulation: 8.