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Trisalus Life Sciences

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233858TriSalus TriGuideTM Guiding CatheterDecember 27, 2023
K230957TriSalus TriNav® LV Infusion SystemMay 2, 2023
K193107TriSalus Infusion SystemDecember 3, 2019