SEIRIN PYONEX ACUPUNCTURE NEEDLES

SEIRIN PYONEX ACUPUNCTURE NEEDLES is an FDA 510(k)-cleared medical device (K970254) manufactured by Seirin-America, Inc.. 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 February 9, 1997. Regulation: 8.