ENDO I/A PROBE

ENDO I/A PROBE is an FDA 510(k)-cleared medical device (K924149) manufactured by Snowden-Pencer. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 1993. Regulation: 8.