3B RESMART BPAP 25A, BMC RESMART BPAP 25A

3B RESMART BPAP 25A, BMC RESMART BPAP 25A is an FDA 510(k)-cleared medical device (K133769) manufactured by 3B Medical, 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 August 24, 2014. Regulation: 8.