
D.T. Davis Enterprises Ltd. T/A Hovertech Int'L
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HT-WEDGE is an FDA 510(k)-cleared medical device (K121287) manufactured by D.T. Davis Enterprises Ltd. T/A Hovertech Int'L. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 2, 2012. Regulation: 8.

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