
Glooko, Inc.
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GLOOKO DEVICE SYSTEM FOR GLOOKO LOGBOOK+ APPLICATION is an FDA 510(k)-cleared medical device (K130886) manufactured by Glooko, 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 April 24, 2013. Regulation: 8.