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Yeou-Fwu Rubber Industrial Co., Ltd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K892946 STERILE PATIENT EXAMINATION GLOVESLYY1989-08-10 View
510(k) K892302 NON-STERILE PATIENT EXAMINATION GLOVESLYY1989-04-28 View
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