7.5 MHZ ENDORECTAL PROBE

7.5 MHZ ENDORECTAL PROBE is an FDA 510(k)-cleared medical device (K881028) manufactured by Philips Ultrasound, 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 April 26, 1988. Regulation: 8.