5.0 MHZ MERIDIAN ULTRASOUND IMAGING SYSTEM

5.0 MHZ MERIDIAN ULTRASOUND IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K860009) manufactured by Johnson & Johnson Professionals, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 19, 1986. Regulation: 8.