PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK

PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK is an FDA 510(k)-cleared medical device (K061975) manufactured by Acmi Corporation. 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 August 9, 2006. Regulation: 8.