RESMART CPAP, RESMART AUTO-CPAP AND RESMART HUMIDIFIER

RESMART CPAP, RESMART AUTO-CPAP AND RESMART HUMIDIFIER is an FDA 510(k)-cleared medical device (K110629) manufactured by 3B Products, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 26, 2012. Regulation: 8.