Z KAT FLUROTACTIC GUIDANCE SYSTEM MKI

Z KAT FLUROTACTIC GUIDANCE SYSTEM MKI is an FDA 510(k)-cleared medical device (K984298) manufactured by Z-Kat, 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 June 22, 1999. Regulation: 8.