NeoWave Pain Relief and Recovery System, Model# T16-2020

NeoWave Pain Relief and Recovery System, Model# T16-2020 is an FDA 510(k)-cleared medical device (K202693) manufactured by Eva Medtec, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 4, 2021. Regulation: 8.