DAN KERRISON RONGEURS, MODELS K1 + BILLY 1

DAN KERRISON RONGEURS, MODELS K1 + BILLY 1 is an FDA 510(k)-cleared medical device (K023868) manufactured by Dannoritzer Medical Instruments. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 6, 2003. Regulation: 8.