DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE

DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE is an FDA 510(k)-cleared medical device (K930751) manufactured by Intl. Medical Consultants. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 2, 1993. Regulation: 8.