CENTAURSET 300 & 300 P.E.D

CENTAURSET 300 & 300 P.E.D is an FDA 510(k)-cleared medical device (K830258) manufactured by Centaur Sciences, Inc.. 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 February 14, 1983. Regulation: 8.