PIONEER ELEC-TROCAR DEVICE

PIONEER ELEC-TROCAR DEVICE is an FDA 510(k)-cleared medical device (K971728) manufactured by Pioneer Surgical Technology. 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 September 18, 1997. Regulation: 8.