DBC, DONG BANG ACUPUNCTURE NEEDLES

DBC, DONG BANG ACUPUNCTURE NEEDLES is an FDA 510(k)-cleared medical device (K990328) manufactured by Morning Star, Dong Bang Acupuncture U.S.A., 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 May 3, 1999. Regulation: 8.