# K153190: Zenysis Short-Term Dialysis Catheter

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Jan 5, 2016 after 63 days
- Product code: MPB (Catheter, Hemodialysis, Non-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: 10 generations back to K001901 (2000). 26 ancestors in all.
No later device cites it as a predicate yet.
5 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010778: Niagara Slim-Cath, C.R. Bard, Inc. (2001) Summary page 4.
- K141531: Power-Trialysis Slim-Cath Short-Term Dialysis Catheter, C.R. Bard, Inc. (2015) Summary page 4.

## Indications for use
The Zenysis™ Short-Term Dialysis Catheter, is indicated for use in attaining short-term (less than 30 days) vascular access for hemodialysis, hemoperfusion, and apheresis treatments. The catheter is intended to be inserted in the jugular, femoral, or subclavian vein as required.

Source page: https://510kreport.com/device/K153190
Methodology: https://510kreport.com/methodology