NICHOLAS II, VIRAL-BACTERIAL FILTER

NICHOLAS II, VIRAL-BACTERIAL FILTER is an FDA 510(k)-cleared medical device (K811546) manufactured by K & G Healthcare Ind., 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 August 2, 1981. Regulation: 8.