CRF CHARCOAL CANISTER REPLACEMENT FILTER

CRF CHARCOAL CANISTER REPLACEMENT FILTER is an FDA 510(k)-cleared medical device (K920209) manufactured by Quinn Healthcare Products. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 30, 1992. Regulation: 8.