# K010838: Fox Pta Catheter, 3.0, 4.0, 5.0, 6.0, 7.0, and 8.0 X 40 MM, Models A14003, A14004, A14005, A14006, A14007, A14008

- Pathway: 510(k) (Traditional)
- Applicant: Jomed AG
- Decided: Jun 21, 2001 after 93 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.
17 later devices descend from it; 2 cite it directly.
0 of 18 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
- K020854: Modification to Fox Pta Catheter (2002), 16 descendants of its own
- K033217: Pheron Pta Catheter (2003), 8 descendants of its own
- K072765: Passeo 18 (2007), 7 descendants of its own
- K082933: Passeo-35 Pta Catheter (2008), 5 descendants of its own
- K040954: Fox Plus Pta Catheter (2004), 5 descendants of its own

Source page: https://510kreport.com/device/K010838
Methodology: https://510kreport.com/methodology