VACUETTE MULTI-SAMPLE NEEDLE

VACUETTE MULTI-SAMPLE NEEDLE is an FDA 510(k)-cleared medical device (K973620) manufactured by Greiner Meditech, 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 December 16, 1997. Regulation: 8.