
Rehabilicare, Inc.
Free shipping on orders over $99 · 30-day returns
PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT is an FDA 510(k)-cleared medical device (K011017) manufactured by Rehabilicare, 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 September 23, 2001. Regulation: 8.