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Ichor

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K233917ICHOR 7F Embolectomy System (ICH-7F)July 18, 2024
K230743ICHOR 14F Embolectomy SystemSeptember 5, 2023