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Seyen Intl., Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K900790 PROTEX LATEX EXAMINATION GLOVELYY1990-04-05 View
510(k) K900933 PROTEX LATEX EXAMINATION GLOVESLYY1990-03-27 View
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