
Teratech Corp.
Free shipping on orders over $99 · 30-day returns
TERATECH MODEL 8EC4 ENDOCAVITY SMART PROBE is an FDA 510(k)-cleared medical device (K010883) manufactured by Teratech Corp.. 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 5, 2001. Regulation: 8.