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Abk Biomedical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K234123
Easi-Vue® embolic microspheres System
February 13, 2024
K220567
Easi-Vue embolic microspheres System
September 7, 2022