SENORX BIOPSY DEVICE II

SENORX BIOPSY DEVICE II is an FDA 510(k)-cleared medical device (K040842) manufactured by Senorx, 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 April 29, 2004. Regulation: 8.