Neptune Medical, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K240853Pathfinder® CR SystemJune 27, 2024
K230801Pathfinder Endoscope Overtube with Balloon DeviceJuly 28, 2023
K211301Pathfinder Endoscope OvertubeMay 28, 2021
K210915Pathfinder Endoscope CapMay 25, 2021
K191415Pathfinder Endoscope OvertubeAugust 30, 2019