TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR SE-30 TENS

TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR SE-30 TENS is an FDA 510(k)-cleared medical device (K991397) manufactured by Sein Electronics Co., Ltd.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 10, 2000. Regulation: 8.