GEISTER SURGICAL INT'L MONOPOLAR ENDOSCOPIC SURG.INST.

GEISTER SURGICAL INT'L MONOPOLAR ENDOSCOPIC SURG.INST. is an FDA 510(k)-cleared medical device (K933300) manufactured by Lyle Howard Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 29, 1994. Regulation: 8.