ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATH

ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATH is an FDA 510(k)-cleared medical device (K883763) manufactured by Acme-Monaco Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 17, 1988. Regulation: 8.