FAST START TENS, MODEL FS 3001

FAST START TENS, MODEL FS 3001 is an FDA 510(k)-cleared medical device (K041092) manufactured by Vision Quest Industries, 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 June 30, 2004. Regulation: 8.