ELECTRO-NERVE STIMULATOR TENS, MODEL LX

ELECTRO-NERVE STIMULATOR TENS, MODEL LX is an FDA 510(k)-cleared medical device (K990230) manufactured by Biomedical Life Systems, 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 August 18, 1999. Regulation: 8.