GHAJAR GUIDE SYSTEM FOR THE PERFORATOR

GHAJAR GUIDE SYSTEM FOR THE PERFORATOR is an FDA 510(k)-cleared medical device (K875019) manufactured by Neurodynamics, 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 January 21, 1988. Regulation: 8.