Medflow Corp., Inc.
Country not established
- Devices
- 1
What Medflow Corp., Inc. makes
Medflow Corp., Inc. manufactures the MEDIRESP III, a medical device designed for respiratory monitoring and patient assessment, likely used in clinical or home healthcare settings to track breathing patterns and oxygen levels.
The MEDIRESP III is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Mediresp Iii Ref K924272
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medflow Corp., Inc. have in the registry?
The registry currently lists 1 device for Medflow Corp., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medflow Corp., Inc.'s devices?
Among its 1 most recently registered device, Medflow Corp., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medflow Corp., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medflow Corp., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medflow Corp., Inc. in the registry?
The most recently registered devices listed for Medflow Corp., Inc. include MEDIRESP III.