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AIOBIO 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
K221275
Qraycam PRO
September 4, 2024
K183121
Qraypen
July 18, 2019