# K130397: Arrow Gpscath Balloon Dilatation Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Hotspur Technologies
- Decided: Jun 20, 2013 after 121 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 K014212 (2002). 4 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113769: Gpscath Ballon Dilatation Catheter, Hotspur Technologies (2012) Summary page 1.

## Most influential descendants
- K151678: Chameleon PTA Balloon Catheter (2015), 2 descendants of its own
- K163231: Chameleon PTA Balloon Catheter (2017), 1 descendant of its own
- K170635: Chameleon PTA Balloon Catheter (2017), 0 descendants of its own

## Indications for use
The Arrow GPSCath Balloon 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. This catheter is not for use in coronary arteries.

Source page: https://510kreport.com/device/K130397
Methodology: https://510kreport.com/methodology