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Foshan Nanhai Bai HE Medical Technology Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K102833DISPOSABLE HEMODIALYSIS ACCESS CATHETER SETSNovember 18, 2011
K070451ABLE CENTRAL VENOUS CATHETERJuly 31, 2007