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Guangzhou Pinzhi Medical Technology Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250033Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)April 7, 2025