MILLER PERCUTANEOUS ANGIOGRAPHIC/SCOPIC IRRI. CATH

MILLER PERCUTANEOUS ANGIOGRAPHIC/SCOPIC IRRI. CATH is an FDA 510(k)-cleared medical device (K897051) manufactured by Cathlab Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 15, 1990. Regulation: 8.