# K001992: Ilt 0.014 Catheter, Model C114NL2

- Pathway: 510(k) (Traditional)
- Applicant: Intra Luminal Therapeutics, Inc.
- Decided: Sep 25, 2000 after 88 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.
158 later devices descend from it; 5 cite it directly.
1 of 159 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
- K012169: Ilt Support Catheter .014, Model C114LW1; Ilt Support Catheter Advancing Mechanism, Model A11AM1 (2001), 123 descendants of its own
- K030984: Safe Cross Angled Support 0.14, Safe Cross Straight Support Catheter 0.14, Safe Cross Angled Support Catheter, Safe Crot (2003), 122 descendants of its own
- K032660: Xtrak Support Catheter (2003), 120 descendants of its own
- K051772: Asahi Tornus Support Catheter (2005), 119 descendants of its own
- K011562: Lumend Percutaneous Catheter (2002), 105 descendants of its own

Source page: https://510kreport.com/device/K001992
Methodology: https://510kreport.com/methodology