NEUROMED MODEL 1992 LS LAMITRODE LEAD

NEUROMED MODEL 1992 LS LAMITRODE LEAD is an FDA 510(k)-cleared medical device (K905255) manufactured by Neuromed, 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 24, 1991. Regulation: 8.