3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031

3.0 MHZ LINEAR ARRAY PROBE MODEL UST 5031 is an FDA 510(k)-cleared medical device (K860313) manufactured by Johnson & Johnson Professionals, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 16, 1986. Regulation: 8.