FDA 510(k) Applications Submitted by Neptune Medical, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K230801 03/23/2023 Pathfinder Endoscope Overtube with Balloon Device Neptune Medical, Inc.
K210915 03/29/2021 Pathfinder Endoscope Cap Neptune Medical, Inc.
K211301 04/29/2021 Pathfinder Endoscope Overtube Neptune Medical, Inc.
K191415 05/28/2019 Pathfinder Endoscope Overtube Neptune Medical, Inc.


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