WIMRT MODULE FOR ARTP PLANNING SYSTEM

WIMRT MODULE FOR ARTP PLANNING SYSTEM is an FDA 510(k)-cleared medical device (K041971) manufactured by Prodigm Group, 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 May 19, 2005. Regulation: 8.