MONOJECT MENGHINI SOFT TISSUE BIOPSY

MONOJECT MENGHINI SOFT TISSUE BIOPSY is an FDA 510(k)-cleared medical device (K843264) manufactured by Sherwood Medical Co.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 1984. Regulation: 8.