SIEMEN'S SIREMOBILE II C-ARM

SIEMEN'S SIREMOBILE II C-ARM is an FDA 510(k)-cleared medical device (K902983) manufactured by Electromek Diagnostic Systems, 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 November 5, 1990. Regulation: 8.