UROSKOP D1, UROSKOP D2, AND UROSKOP D3

UROSKOP D1, UROSKOP D2, AND UROSKOP D3 is an FDA 510(k)-cleared medical device (K923049) manufactured by Siemens Medical Solutions USA, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 14, 1992. Regulation: 8.