HEWLETT PACKARD CONOS ULTRASOUND IMAGING SYSTEM MODIFICATION

HEWLETT PACKARD CONOS ULTRASOUND IMAGING SYSTEM MODIFICATION is an FDA 510(k)-cleared medical device (K934041) manufactured by Hewlett-Packard Co.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 21, 1994. Regulation: 8.