Acapella Choice Blue Vibratory PEP Device

Acapella Choice Blue Vibratory PEP Device is an FDA 510(k)-cleared medical device (K181660) manufactured by Smiths Medical. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 23, 2019. Regulation: 8.