
Greiner Bio-One North America, Inc.
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MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES is an FDA 510(k)-cleared medical device (K063357) manufactured by Greiner Bio-One 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 July 9, 2007. Regulation: 8.