MSLS6QF TENS/PMS Device

MSLS6QF TENS/PMS Device is an FDA 510(k)-cleared medical device (K193655) manufactured by Self Doctor Care, LLC. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 3, 2020. Regulation: 8.