# K862117: Tracker Infusion Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Target Therapeutics
- Decided: Oct 1, 1986 after 120 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.
9 later devices descend from it; 3 cite it directly.
0 of 10 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
- K151638: Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter (2015), 6 descendants of its own
- K180959: Phenom 27 Catheter (2018), 4 descendants of its own
- K210230: Phenom Catheters (2021), 2 descendants of its own
- K260199: SLIM Microcatheter (2026), 0 descendants of its own
- K251668: SurfRider 13 Microcatheter (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K862117
Methodology: https://510kreport.com/methodology