SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIO

SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIO is an FDA 510(k)-cleared medical device (K926271) manufactured by Schneider Intl., Ltd.. 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 6, 1993. Regulation: 8.