PBN FALLOPIAN TUBE CATHETER SYSTEM

PBN FALLOPIAN TUBE CATHETER SYSTEM is an FDA 510(k)-cleared medical device (K000620) manufactured by Medical Device Technologies, Inc.. 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 October 29, 2000. Regulation: 8.