RESPIRADYNE II(TM)

RESPIRADYNE II(TM) is an FDA 510(k)-cleared medical device (K863866) manufactured by Chesebrough-Pond'S U.S.A. Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 27, 1987. Regulation: 8.