ACCU-BEAM TISSUE DRILL & ASPIRATION/INJECTION NEEDLE

ACCU-BEAM TISSUE DRILL & ASPIRATION/INJECTION NEEDLE is an FDA 510(k)-cleared medical device (K934398) manufactured by Transamerican Technologies Intl.. 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 February 13, 1994. Regulation: 8.