ANGIO-FLO CONTIN-ARTERIAL FLUSH DEV.

ANGIO-FLO CONTIN-ARTERIAL FLUSH DEV. is an FDA 510(k)-cleared medical device (K832058) manufactured by Parke-Davis Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 11, 1983. Regulation: 8.