MEDLINE TITANIUM HEMOCLIPS

MEDLINE TITANIUM HEMOCLIPS is an FDA 510(k)-cleared medical device (K962016) manufactured by Medline Industries, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 23, 1996. Regulation: 8.