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Ultroid, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K030315 MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEMKNS2003-02-27 View
510(k) K023706 ULTROID HEMORRHOID MANAGEMENT SYSTEMKNS2003-01-14 View
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