RADIONICS SLUIJTER-MEHTA CANNULA

RADIONICS SLUIJTER-MEHTA CANNULA is an FDA 510(k)-cleared medical device (K963577) manufactured by Radionics, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 1996. Regulation: 8.