# Angiometrx, Inc.

- Location (FDA's records): Vancouver, Bc, CA
- FDA decisions: 3 (2003–2005): 3 510(k) clearances
- Product codes: DQO (2), LIT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Mediguide, Ltd.: 1 (https://510kreport.com/company/mediguide)
- Endocross, Ltd.: 1 (https://510kreport.com/company/endocross)

## Its most-cited devices
- K024000: Metricath System Comprised of Metricath 1000 Console & Metricath Balloon Catheter (2003), cited by 1
- K042685: Metricath System (2004), cited by 1

## Recent decisions
- K051042: Metricath Gemini-P Balloon Catheter, Models RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, Metricath Console, Model 1000 (Aug 5, 2005)
- K042685: Metricath System (Nov 18, 2004)
- K024000: Metricath System Comprised of Metricath 1000 Console & Metricath Balloon Catheter (Jun 26, 2003)

Source page: https://510kreport.com/company/angiometrx