SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES

SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES is an FDA 510(k)-cleared medical device (K963769) 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 October 15, 1996. Regulation: 8.