CORDIS PTCA GUIDING CATHETER, MODIFICATION

CORDIS PTCA GUIDING CATHETER, MODIFICATION is an FDA 510(k)-cleared medical device (K913783) manufactured by Dow Corning Wright. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 17, 1991. Regulation: 8.