LICHEN, BACTERIAL IN LINE BREATHING FILTER

LICHEN, BACTERIAL IN LINE BREATHING FILTER is an FDA 510(k)-cleared medical device (K980662) manufactured by Dhd Healthcare Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 1998. Regulation: 8.