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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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