Pathfinder® CR System— 510(k) K240853

Name: FDA 510(k) clearance K240853
Creator: U.S. Food and Drug Administration
Published: 2024-06-27

Unknown

Neptune Medical, Inc.

FDA 510(k) clearance K240853 for Pathfinder® CR System, Unknown on 2024-06-27. Applicant: Neptune Medical, Inc.. Device class: 2.

Clearance details

Applicant: Neptune Medical, Inc.
Product code: Code FED
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2024-03-28
Decision date: 2024-06-27
Decision: Unknown
Clearance type: Traditional
Location: Burlingame, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Neptune Medical, Inc.

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K260503 — Triton 1 System2026-09-03
K230801 — Pathfinder Endoscope Overtube with Balloon Device2023-07-28
K211301 — Pathfinder Endoscope Overtube2021-05-28
K210915 — Pathfinder Endoscope Cap2021-05-25
K191415 — Pathfinder Endoscope Overtube2019-08-30

Adverse events under product code FED

product code FED

Death: 10
Total: 10

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.