Resonic Rapid Acoustic Pulse Device

Resonic Rapid Acoustic Pulse Device is an FDA 510(k)-cleared medical device (K222629) manufactured by Zeltiq Aesthetics, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 24, 2022. Regulation: 8.