MODIFIED PERIPHERAL DILATATION CATHETERS

MODIFIED PERIPHERAL DILATATION CATHETERS is an FDA 510(k)-cleared medical device (K875175) manufactured by Schneider-Shilley (Usa). This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 27, 1988. Regulation: 8.