NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF

NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF is an FDA 510(k)-cleared medical device (K905101) 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 December 19, 1990. Regulation: 8.