# K003972: Numed Ghost II Pta Catheters

- Pathway: 510(k) (Special)
- Applicant: NuMED, Inc.
- Decided: Jan 11, 2001 after 20 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- 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.
20 later devices descend from it; 3 cite it directly.
0 of 21 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/K003972
Methodology: https://510kreport.com/methodology