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Neurophet., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252496Neurophet AQUA AD PlusJanuary 29, 2026
K242215Neurophet AQUA (V3.1)October 25, 2024
K220437Neurophet AQUAMay 10, 2023
K221405Neurophet SCALE PETAugust 5, 2022