WESTMED CIRCULARIE PEP DEVICES

WESTMED CIRCULARIE PEP DEVICES is an FDA 510(k)-cleared medical device (K955047) manufactured by Westmed Intl.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 26, 1996. Regulation: 8.