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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K890592 PATIENT EXAMINATION GLOVELYY1989-05-22 View
510(k) K891885 PATIENT EXAMINATION GLOVES (LATEX)LYY1989-04-11 View
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