RSI-MRI+

RSI-MRI+ is an FDA 510(k)-cleared medical device (K191278) manufactured by Multimodal Imaging Services Corporation (Dba Healthlytix). 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 18, 2019. Regulation: 8.