CENTROS CHRONIC HEMODIALYSIS CATHETER SET— 510(k) K092597

Unknown

Ash Access Technology, Inc.

FDA 510(k) clearance K092597 for CENTROS CHRONIC HEMODIALYSIS CATHETER SET, Unknown on 2009-11-12. Applicant: Ash Access Technology, Inc..

Clearance details

Applicant: Ash Access Technology, Inc.
Product code: Code MSD
Advisory panel: Gastroenterology, Urology
Date received: 2009-08-24
Decision date: 2009-11-12
Decision: Unknown
Clearance type: Traditional
Location: Lafayette, IN, US

Download summary PDF View on FDA.gov ↗

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.