INTRAVENOUS CATHETERS MODIFICATIONS

INTRAVENOUS CATHETERS MODIFICATIONS is an FDA 510(k)-cleared medical device (K921295) manufactured by Critikon Company, LLC. 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 May 16, 1993. Regulation: 8.