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Fcu Co., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K233579
SC1 Handheld Ultrasound Imaging system (Model: SC1)
June 26, 2024
K210468
SC1 Handheld Ultrasound Imaging System (Model: SC1)
July 23, 2021