
Haemoscope Corp.
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THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY is an FDA 510(k)-cleared medical device (K041502) manufactured by Haemoscope Corp.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 31, 2004. Regulation: 8.