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Disa Medinotec

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K241562OutFlo Aortic Valve Dilatation Balloon CatheterMarch 11, 2025
K211894TrachealatorNovember 24, 2021