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Profound Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K240296Tulsa Pro System (Pad-105)May 9, 2024
K230692TULSA-PRO SystemSeptember 20, 2023
K211858TULSA-PRO SystemSeptember 6, 2022
K202286Tulsa-Pro SystemSeptember 16, 2020
K191200TULSA-PRO SystemAugust 15, 2019