UNIBLATE ELECTROSURGICAL DEVICE

UNIBLATE ELECTROSURGICAL DEVICE is an FDA 510(k)-cleared medical device (K080451) manufactured by AngioDynamics, 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 2, 2008. Regulation: 8.