MONITORING KIT, CENTRAL VENOUS PRESSURE

MONITORING KIT, CENTRAL VENOUS PRESSURE is an FDA 510(k)-cleared medical device (K770290) manufactured by Argon Medical 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 March 14, 1977. Regulation: 8.