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Chungwoo Co., Ltd.

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

Total Devices2
Categories1
Latest Approval2024-05-23
TypeNumberDevice NameCodeDate
510(k) K233120 CWM-930S, FIXER DV9 GEI 2024-05-23 View
510(k) K222709 Retraction, CWM-910T, APOLEX Tite GEI 2023-03-21 View