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Jiangxi Yikang Medical Instrument Group Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K190213Yikang Endotracheal TubeSeptember 6, 2019
K173340Yikang Latex Foley CatheterJuly 13, 2018