FUTURECARE CARELYNK IV SYSTEM

FUTURECARE CARELYNK IV SYSTEM is an FDA 510(k)-cleared medical device (K903512) manufactured by Futurecare Systems, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 17, 1991. Regulation: 8.