ELECTRICAL MUSCLE STIMULATOR--PGS 2000 TENS DEVICE

ELECTRICAL MUSCLE STIMULATOR--PGS 2000 TENS DEVICE is an FDA 510(k)-cleared medical device (K895760) manufactured by Universal Technology Systems, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 1, 1990. Regulation: 8.