Metriflow, Inc.
Country not established
- Devices
- 1
What Metriflow, Inc. makes
Metriflow, Inc. manufactures the AFM-100, a peripheral vascular blood flow meter designed to measure blood flow in extremities. The device is intended for clinical use in assessing circulatory function, particularly in vascular studies or monitoring conditions affecting limb perfusion.
The AFM-100 is classified as a Class II medical device under FDA regulations and is subject to 510(k) clearance. The device is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Metriflow, Inc. have in the registry?
The registry currently lists 1 device for Metriflow, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Metriflow, Inc.'s devices?
Among its 1 most recently registered device, Metriflow, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Metriflow, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Metriflow, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Metriflow, Inc. in the registry?
The most recently registered devices listed for Metriflow, Inc. include METRIFLOW AFM-100 PERIPHERAL VASCULAR BLOOD FLOWME.