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Fem Suite, LLC

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K093218 FEMEYE TWOHIH2010-05-18 View
510(k) K062563 FEMTEN CERVICAL TENACULUMHDC2007-05-18 View
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