LS SERIES 200 FLOVISION SYSTEM

LS SERIES 200 FLOVISION SYSTEM is an FDA 510(k)-cleared medical device (K971981) manufactured by Systam. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 21, 1998. Regulation: 8.