MAB — Marker, Cardiopulmonary Bypass (Vein Marker) Class II

FDA Device Classification

FDA product code MAB covers "Marker, Cardiopulmonary Bypass (Vein Marker)", a Class II medical device regulated under 21 CFR 870.3450. Submissions are reviewed by the Cardiovascular panel. At least 3 recent 510(k) clearances have been granted under this product code.