CORSON MYOMA GRASPING FORCEPS

CORSON MYOMA GRASPING FORCEPS is an FDA 510(k)-cleared medical device (K926484) manufactured by Thomasville Medical Assoc.. 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 February 24, 1994. Regulation: 8.