INFUSION SETS #'S 124 & 142 PERSONAL

INFUSION SETS #'S 124 & 142 PERSONAL is an FDA 510(k)-cleared medical device (K831445) manufactured by Pacesetter Systems. 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 11, 1983. Regulation: 8.