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Percuvision, LLC

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K091600 DIRECTVISION GUIDE SYSTEMFGC2009-08-25 View
510(k) K090262 PERCUCATH URINARY CATHETEREZL2009-05-28 View
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