MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR

MODEL HP (OR MODEL 1001) TRANSCUTANEOUS STIMULATOR is an FDA 510(k)-cleared medical device (K871666) manufactured by Oriental Medical Supplies, 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 June 24, 1987. Regulation: 8.