MODEL 19 STIMULATOR, NERVE, TRANSCUTANEOUS

MODEL 19 STIMULATOR, NERVE, TRANSCUTANEOUS is an FDA 510(k)-cleared medical device (K925898) manufactured by Staodyne, 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 27, 1993. Regulation: 8.