ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE

ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE is an FDA 510(k)-cleared medical device (K812685) manufactured by Ericka. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 28, 1981. Regulation: 8.