HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS

HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS is an FDA 510(k)-cleared medical device (K842829) manufactured by North American Instrument 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 October 17, 1984. Regulation: 8.