# K092597: Centros Chronic Hemodialysis Catheter Set

- Pathway: 510(k) (Traditional)
- Applicant: Ash Access Technology, Inc.
- Decided: Nov 12, 2009 after 80 days
- Product code: MSD (Catheter, Hemodialysis, Implanted)
- Device class: 2
- Regulation: 21 CFR 876.5540
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K981994 (1998). 15 ancestors in all.
2 later devices descend from it; 1 cites it directly.
1 of 18 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070572: Ash Advance Hemodialysis Catheter and Procedure Kit, Models; 15FR X 24CM, 15FR X 28CM, 15FR X 32CM, Ash Access Technology, Inc. (2007) Summary page 1.
- K080400: Angiodynamics, Inc., Duramax Hemodialysis Catheter and Procedure Kit, AngioDynamics, Inc. (2008) Summary page 1.
- K040402: Angiodynamics, Inc. More-Flow Hemodialysis Catheter and Procedure Kit, AngioDynamics, Inc. (2004) Summary page 1.

## Most influential descendants
- K141363: Centros Long Term Hemodialysis Catheter, Centrosflo Long Term Hemodialysis Catheter (2014), 1 descendant of its own
- K151967: Centros Long-Term Hemodialysis Catheter, CentrosFLO Long-Term Hemodialysis Catheter (2016), 0 descendants of its own

## Indications for use
The CentrosTM Chronic Hemodialysis Catheter Set is indicated for use in attaining long-term vascular access for hemodialysis and apheresis. It may be inserted percutaneously and is primarily placed in the internal jugular vein of an adult patient. This catheter is indicated for> 30 days long-term placement.

Source page: https://510kreport.com/device/K092597
Methodology: https://510kreport.com/methodology