D.T. Davis Enterprises Ltd. T/A Hovertech Int'L is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
D.T. Davis Enterprises Ltd. T/A Hovertech Int'L - FDA 510(k) Cleared ...
2
Total
2
Cleared
0
Denied
D.T. Davis Enterprises Ltd. T/A Hovertech Int'L has 2 FDA 510(k) cleared medical devices. Based in Bethlehem, US.
Historical record: 2 cleared submissions from 2010 to 2012. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by D.T. Davis Enterprises Ltd. T/A Hovertech Int'L Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - D.T. Davis Enterprises Ltd. T/A Hovertech Int'L
2 devices