# K051343: Mini Ghost Pta Catheter, Model 507

- Pathway: 510(k) (Special)
- Applicant: NuMED, Inc.
- Decided: Jul 28, 2005 after 66 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K0931009: NuMED Z-MED PTA Catheter. Number could not be read

## Most influential descendants
- K130414: Chocolate Pta Balloon Catheter (Over the Wire) 0.014 Guide Wire, Chocolate Pta Balloon Catheter (Over the Wire) 0.018 (2013), 1 descendant of its own
- K213631: Chocolate PTA Balloon Catheter (2021), 0 descendants of its own

## Indications for use
This catheter is recommended for Percutaneous Transluminal Angioplasty (PTA) of the femoral, iliac, and renal arteries. These catheters are not designed to be used in the coronary arteries.

Source page: https://510kreport.com/device/K051343
Methodology: https://510kreport.com/methodology