# K881743: Vas-Cath Flexxicon Dual Lumen Dialysis Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Vas-Cath, Inc.
- Decided: Jun 23, 1988 after 62 days
- Product code: LFJ (Catheter, Subclavian)
- 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
1 of 3 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K090102: Niagara, Niagara Slim-Cath, and Brevia Short-Term Curved Extension Hemodialysis Catheters (2009), 1 descendant of its own
- K102833: Disposable Hemodialysis Access Catheter Sets (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K881743
Methodology: https://510kreport.com/methodology