OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER

OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER is an FDA 510(k)-cleared medical device (K973013) manufactured by Vas-Cath, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 18, 1998. Regulation: 8.