INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE

INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE is an FDA 510(k)-cleared medical device (K994252) manufactured by Boston Scientific 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 January 3, 2000. Regulation: 8.