# K041093: Numed Mullins X Pta Catheter

- Pathway: 510(k) (Special)
- Applicant: NuMED, Inc.
- Decided: May 6, 2004 after 9 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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 Mullins X PTA Catheter: named in the summary without a submission number

## Most influential descendants
- K082868: Mullins-X, Model 250X (2008), 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/K041093
Methodology: https://510kreport.com/methodology