REPLACABLE BATTERY PERFECTEMP CAUTERY

REPLACABLE BATTERY PERFECTEMP CAUTERY is an FDA 510(k)-cleared medical device (K810016) manufactured by Medical Products Development, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 22, 1981. Regulation: 8.