SIEMENS MAIN FLOW BACTERIA FILTER

SIEMENS MAIN FLOW BACTERIA FILTER is an FDA 510(k)-cleared medical device (K871366) manufactured by Siemens Elema AB. 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 13, 1987. Regulation: 8.