# K230191: Arise™ UHP Dilatation Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Creagh Medical, Ltd.
- Decided: Mar 22, 2023 after 57 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
Longest line of descent: 4 generations back to K042537 (2004). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102645: Willow/Elm Pta Balloon Dilatation Catheter, Creagh Medical, Ltd. (2010) Summary page 4.

## Indications for use
The UHP Dilatation Catheter is indicated for use in Percutaneous Transluminal Angioplasty of the femoral, iliac and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae.

Source page: https://510kreport.com/device/K230191
Methodology: https://510kreport.com/methodology