INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE

INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE is an FDA 510(k)-cleared medical device (K915696) manufactured by Interspec, 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 November 23, 1992. Regulation: 8.