BARD MINI-INFUSER 1500 & 3000

BARD MINI-INFUSER 1500 & 3000 is an FDA 510(k)-cleared medical device (K930459) manufactured by Bard Medsystems Div.. 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 August 9, 1993. Regulation: 8.