PARI FILTER/VALVE SET

PARI FILTER/VALVE SET is an FDA 510(k)-cleared medical device (K926455) manufactured by Paul Ritzau Pari-Werk GmbH. 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 27, 1993. Regulation: 8.