Abk Biomedical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K234123Easi-Vue® embolic microspheres SystemFebruary 13, 2024
K220567Easi-Vue embolic microspheres SystemSeptember 7, 2022