Angiometrx, Inc.
Country not established
- Devices
- 3
What Angiometrx, Inc. makes
Angiometrx produces percutaneous balloon catheters and integrated console systems for intravascular imaging and measurement, including the METRICATH GEMINI-P series (sizes RX2515S-P through RX4015S-P) and the METRICATH 1000 console. These devices are designed for coronary and peripheral vascular applications to assess vessel dimensions and guide interventional procedures.
The company’s products fall under FDA Class II regulation and are authorised via 510(k) clearance. The devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Metricath System Ref K042685
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiometrx, Inc. have in the registry?
The registry currently lists 3 devices for Angiometrx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiometrx, Inc.'s devices?
Among its 3 most recently registered devices, Angiometrx, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Angiometrx, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Angiometrx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiometrx, Inc. in the registry?
The most recently registered devices listed for Angiometrx, Inc. include METRICATH GEMINI-P BALLOON CATHETER, MODELS RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, METRICATH CONSOLE, MODEL 1000, METRICATH SYSTEM COMPRISED OF METRICATH 1000 CONSOLE & METRICATH BALLOON CATHETER and METRICATH SYSTEM.