STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES

STRYKER ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS & ACCESORIES is an FDA 510(k)-cleared medical device (K935222) manufactured by Stryker Endoscopy. 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 March 24, 1994. Regulation: 8.