# K925979: Dual Lumen L-Cath Catheter System

- Pathway: 510(k) (Traditional)
- Applicant: Luther Medical Products, Inc.
- Decided: May 27, 1993 after 183 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- 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.
0 of 3 devices in its family (counting itself) have 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
- K091670: BD L-Cath Single and Dual Lument Catheters, Midline Catheter (2009), 1 descendant of its own
- K230669: L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K925979
Methodology: https://510kreport.com/methodology