TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER

TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER is an FDA 510(k)-cleared medical device (K971111) manufactured by Tri-Tech, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 15, 1997. Regulation: 8.