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Shenzhen Greatro Electronic 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
K242595Intense Pulse Light Therapeutic Apparatus (IPL-18 BF, IPL-18 FG)November 7, 2024
K232932Intense Pulse Light Therapeutic ApparatusDecember 4, 2023