# K142300: Arrow GPSCath Balloon Dialation Catheter (150 cm)

- Pathway: 510(k) (Special)
- Applicant: Hotspur Technologies, Inc.,
- Decided: Sep 17, 2014 after 30 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: 8 generations back to K001134 (2000). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140351: Arrow Gpscath Balloon Dilatation Catheter, Hotspur Technologies,Inc Subsidiary of Teleflex ME (2014) Summary page 4.

## Most influential descendants
- K143093: 0.018 Arrow GPSCath Balloon Dilatation Catheter (150 cm) (2015), 0 descendants of its own

## Indications for use
The Arrow GPSCath Balloon Dilatation Catheter (150 cm) is indicated for Percutaneous Transluminal Angioplasty (PTA) in the peripheral vasculature, including iliac, femoral, popliteal, infra-popliteal 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/K142300
Methodology: https://510kreport.com/methodology