5.0 MHZ INTRACAVITARY SECTOR PROBE

5.0 MHZ INTRACAVITARY SECTOR PROBE is an FDA 510(k)-cleared medical device (K853711) manufactured by General Electric Co.. 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 December 17, 1985. Regulation: 8.