RADIONICS NASHOLD BIOPSY NEEDLE - SINGLE USE

RADIONICS NASHOLD BIOPSY NEEDLE - SINGLE USE is an FDA 510(k)-cleared medical device (K032054) manufactured by Radionics, A Division of Tyco Healthcare Group LP. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 14, 2003. Regulation: 8.