BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT

BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT is an FDA 510(k)-cleared medical device (K101832) manufactured by Medical Device Technologies, Inc.. 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 August 26, 2010. Regulation: 8.