FLOTEC OXYSAVRR (S)

FLOTEC OXYSAVRR (S) is an FDA 510(k)-cleared medical device (K970371) manufactured by Flotec, 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 July 9, 1997. Regulation: 8.