# Guidepath Medical, Inc.

- Location (FDA's records): Austin, TX
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: DQX (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 12 (12 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)
- Argon Medical Corp.: 1 (https://510kreport.com/company/argon-medical)
- Abbott Vascular: 1 (https://510kreport.com/company/abbott-vascular)

## Recent decisions
- K121398: Charlie Guidewire (Regular), Charlie Guidewire (Stiff) (Dec 13, 2012)

Source page: https://510kreport.com/company/guidepath-medical