SHE-LI TENS STIMULATOR MODEL SL-101 RX

SHE-LI TENS STIMULATOR MODEL SL-101 RX is an FDA 510(k)-cleared medical device (K961809) manufactured by Medi Consultants, 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 February 25, 1997. Regulation: 8.