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Chungwoo Co., Ltd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K233120 CWM-930S, FIXER DV9GEI2024-05-23 View
510(k) K222709 Retraction, CWM-910T, APOLEX TiteGEI2023-03-21 View
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