KHT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE

KHT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE is an FDA 510(k)-cleared medical device (K980469) manufactured by American Institute of Koryo Hand Therapy. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 2, 1998. Regulation: 8.