MICROFUSE MEMBRANE INFUSION CATHETER

MICROFUSE MEMBRANE INFUSION CATHETER is an FDA 510(k)-cleared medical device (K971619) manufactured by E-Med Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 26, 1998. Regulation: 8.