Neptune Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Neptune Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Burlingame, US.
Latest FDA clearance: Jun 2024. Active since 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Neptune Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by AlvaMed, Inc. as regulatory consultant.
5 devices
Cleared
Jun 27, 2024
Pathfinder® CR System
Gastroenterology & Urology
91d
Cleared
Jul 28, 2023
Pathfinder Endoscope Overtube with Balloon Device
Gastroenterology & Urology
127d
Cleared
May 28, 2021
Pathfinder Endoscope Overtube
Gastroenterology & Urology
29d
Cleared
May 25, 2021
Pathfinder Endoscope Cap
Gastroenterology & Urology
57d
Cleared
Aug 30, 2019
Pathfinder Endoscope Overtube
Gastroenterology & Urology
94d