iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System

iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System is an FDA 510(k)-cleared medical device (K221081) manufactured by First Source, 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 June 12, 2022. Regulation: 8.