Medical Device Manufacturer · FR , Paris

Wandercraft SAS - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022
3
Total
3
Cleared
0
Denied

FDA 510(k) cleared devices by Wandercraft SAS Neurology ✕

3 devices
1-3 of 3
Cleared Oct 24, 2025
Atalante X
K250904 · PHL
Neurology · 212d
Cleared Dec 13, 2023
Atalante X
K232077 · PHL
Neurology · 153d
Cleared Dec 29, 2022
Atalante
K221859 · PHL
Neurology · 185d
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