HUNTLEIGH FP5000 SYSTEM MODEL FP5000

HUNTLEIGH FP5000 SYSTEM MODEL FP5000 is an FDA 510(k)-cleared medical device (K965153) manufactured by Huntleigh Healthcare, 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 January 25, 1998. Regulation: 8.