# K010531: Ilt Deflecting Catheter, Model C114ND1

- Pathway: 510(k) (Special)
- Applicant: Intra Luminal Therapeutics, Inc.
- Decided: Apr 18, 2001 after 54 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.
32 later devices descend from it; 2 cite it directly.
0 of 33 devices in its family (counting itself) have 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
- K031692: Safe-Cross Deflecting Catheter, Model C114ND1 (2003), 30 descendants of its own
- K032784: Ilt Safe-Cross Deflecting Catheter, Model C114ND1 (2003), 27 descendants of its own
- K040481: Safe-Cross Deflecting Catheter, Model C118ND1 (2004), 26 descendants of its own
- K062769: Pressurewire Certus, Models 12006 and 12306 (2006), 25 descendants of its own
- K080813: Pressurewire Certus, Certus (300CM), Aeris, Aeris (300CM), Receiver (2008), 13 descendants of its own

Source page: https://510kreport.com/device/K010531
Methodology: https://510kreport.com/methodology