SIEMENS ENDO-P-PROBE

SIEMENS ENDO-P-PROBE is an FDA 510(k)-cleared medical device (K897098) manufactured by Siemens Medical Solutions USA, 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 February 22, 1990. Regulation: 8.