MEDIPART FILTER & TUBING MP-02X

MEDIPART FILTER & TUBING MP-02X is an FDA 510(k)-cleared medical device (K844491) manufactured by Medipart Jerry Alexander. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 3, 1984. Regulation: 8.