7.5 MHZ TRANSRECTAL (ENDORECTAL) PROBE

7.5 MHZ TRANSRECTAL (ENDORECTAL) PROBE is an FDA 510(k)-cleared medical device (K870748) 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 9, 1987. Regulation: 8.