# K914162: Vas-Cath Flexxicon 2 Dual Lumen Dialysis Catheters

- Pathway: 510(k) (Traditional)
- Applicant: Vas-Cath, Inc.
- Decided: Jul 1, 1993 after 653 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.
1 later device descends from it; 1 cites it directly.
1 of 2 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K030268: Niagara Temporary Dual Lumen Catheters; Flexxicon II Temporary Dual Lumen Catheters (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K914162
Methodology: https://510kreport.com/methodology