POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER

POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER is an FDA 510(k)-cleared medical device (K965020) manufactured by Porous Media 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 March 13, 1997. Regulation: 8.