CODE #94315 RETROGRADE CORONARY SINUS PERF CANNULA

CODE #94315 RETROGRADE CORONARY SINUS PERF CANNULA is an FDA 510(k)-cleared medical device (K901074) manufactured by Dlp, 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 July 5, 1990. Regulation: 8.