# K082524: Mini Ghost, Model: 507

- Pathway: 510(k) (Special)
- Applicant: NuMED, Inc.
- Decided: Sep 26, 2008 after 24 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) NuMED Mini Ghost PTA Catheter: named in the summary without a submission number

## 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/K082524
Methodology: https://510kreport.com/methodology