HEWLETT-PACKARD CENTRALVUE SOFTWARE

HEWLETT-PACKARD CENTRALVUE SOFTWARE is an FDA 510(k)-cleared medical device (K964832) manufactured by Hewlett-Packard Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 14, 1997. Regulation: 8.