V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER

V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER is an FDA 510(k)-cleared medical device (K953300) manufactured by Hdc Corp.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 29, 1996. Regulation: 8.