SANDER'S MASKCPAP BY RESPIRONICS

SANDER'S MASKCPAP BY RESPIRONICS is an FDA 510(k)-cleared medical device (K851396) manufactured by Respironics, 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 May 14, 1985. Regulation: 8.