STIMTECH SD PATIENT 6089 #78-8050

STIMTECH SD PATIENT 6089 #78-8050 is an FDA 510(k)-cleared medical device (K844213) manufactured by Codman & Shurtleff, 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 9, 1985. Regulation: 8.