IUR RECIPROCATING MORCELLATOR MODEL # 7210517

IUR RECIPROCATING MORCELLATOR MODEL # 7210517 is an FDA 510(k)-cleared medical device (K041774) manufactured by Smith & Nephew, 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 6, 2004. Regulation: 8.