Flume Catheter— 510(k) K231101

Name: FDA 510(k) clearance K231101
Creator: U.S. Food and Drug Administration
Published: 2023-06-29

Substantially Equivalent

Flume Catheter Company, Ltd.

FDA 510(k) clearance K231101 for Flume Catheter, Substantially Equivalent on 2023-06-29. Applicant: Flume Catheter Company, Ltd.. Device class: 2.

Clearance details

Applicant: Flume Catheter Company, Ltd.
Product code: Code EZL
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 2023-04-18
Decision date: 2023-06-29
Decision: Substantially Equivalent
Clearance type: Special
Location: Farnham, GB

Download summary PDF View on FDA.gov ↗

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Adverse events under product code EZL

product code EZL

Death: 6
Injury: 796
Malfunction: 4,989
Other: 1
Total: 5,792

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.