SYMETREX LONG TERM HEMODIALYSIS CATHETER— 510(k) K140884

Name: FDA 510(k) clearance K140884
Creator: U.S. Food and Drug Administration
Published: 2014-11-26

Unknown

Phase One Medical

FDA 510(k) clearance K140884 for SYMETREX LONG TERM HEMODIALYSIS CATHETER, Unknown on 2014-11-26. Applicant: Phase One Medical. Device class: 2.

Clearance details

Applicant: Phase One Medical
Product code: Code MSD
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 2014-04-07
Decision date: 2014-11-26
Decision: Unknown
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MSD

product code MSD

Death: 67
Injury: 545
Malfunction: 3,661
Total: 4,273

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.