COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM

COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM is an FDA 510(k)-cleared medical device (K940484) 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 April 18, 1994. Regulation: 8.