# K991601: Dual Lumen Catheter, Model DL-35-90

- Pathway: 510(k) (Traditional)
- Applicant: Endologix, Inc.
- Decided: Oct 28, 1999 after 171 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- 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.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K080360: Endologix Visiflex Dual Lumen Catheter (2008), 0 descendants of its own

## Indications for use
For use during a two guidewire procedure

Source page: https://510kreport.com/device/K991601
Methodology: https://510kreport.com/methodology