ROHNAR 7000 DIGITAL DIAGN ULTRASOUND

ROHNAR 7000 DIGITAL DIAGN ULTRASOUND is an FDA 510(k)-cleared medical device (K791505) manufactured by Roche Scientific Corp.. 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 16, 1979. Regulation: 8.