# Hotspur Technologies

- Location (FDA's records): Mountain View, CA
- FDA decisions: 7 (2010–2015): 7 510(k) clearances
- Names in FDA's records: Hotspur Technologies (5); Hotspur Technologies, Inc., (2)
- Product codes: LIT (5), DXE (2)
- Predicates its devices cite: 9 (3 its own); citations of its devices by later devices: 5 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Hotspur Technologies,Inc Subsidiary of Teleflex ME: 2 (https://510kreport.com/company/hotspur-technologies-subsidiary-of-teleflex-me)
- Baxter Healthcare Corp: 2 (https://510kreport.com/company/baxter-healthcare)
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)

## Firms that cite its devices most
- Av Medical Technologies, Ltd.: 1 (https://510kreport.com/company/av-medical-technologies)
- Inari Medical, Inc.: 1 (https://510kreport.com/company/inari-medical)

## Its most-cited devices
- K142300: Arrow GPSCath Balloon Dialation Catheter (150 cm) (2014), cited by 1
- K130397: Arrow Gpscath Balloon Dilatation Catheter (2013), cited by 1
- K101047: Pta-Duo Pta Balloon Catheter (2010), cited by 1
- K113769: Gpscath Ballon Dilatation Catheter (2012), cited by 1
- K100842: Pta-Plus Pta Balloon Cather 5 MM X 4CM, Pta-Plus Pta Balloon Catheter 6MM X 4CM (2010), cited by 1

## Recent decisions
- K143093: 0.018 Arrow GPSCath Balloon Dilatation Catheter (150 cm) (Jun 24, 2015)
- K142300: Arrow GPSCath Balloon Dialation Catheter (150 cm) (Sep 17, 2014)
- K130397: Arrow Gpscath Balloon Dilatation Catheter (Jun 20, 2013)
- K113769: Gpscath Ballon Dilatation Catheter (Jan 20, 2012)
- K101047: Pta-Duo Pta Balloon Catheter (Jul 13, 2010)
- K100840: Embo Plus Embolectomy Catheter (Jul 12, 2010)
- K100842: Pta-Plus Pta Balloon Cather 5 MM X 4CM, Pta-Plus Pta Balloon Catheter 6MM X 4CM (Jul 12, 2010)

Source page: https://510kreport.com/company/hotspur-technologies