
Greiner Vacuette North America, Inc.
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VACUETTE EDTA K2 GEL TUBES is an FDA 510(k)-cleared medical device (K012043) manufactured by Greiner Vacuette North America, 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 September 23, 2001. Regulation: 8.