Fluid Motion Biotechnologies, Inc.
Country not established
- Devices
- 1
What Fluid Motion Biotechnologies, Inc. makes
Fluid Motion Biotechnologies, Inc. manufactures the E-Z FLEX, a device designed for medical or procedural use in flexible tubing applications.
The E-Z FLEX is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
E-Z Flex Ref K953456
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fluid Motion Biotechnologies, Inc. have in the registry?
The registry currently lists 1 device for Fluid Motion Biotechnologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fluid Motion Biotechnologies, Inc.'s devices?
Among its 1 most recently registered device, Fluid Motion Biotechnologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fluid Motion Biotechnologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fluid Motion Biotechnologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fluid Motion Biotechnologies, Inc. in the registry?
The most recently registered devices listed for Fluid Motion Biotechnologies, Inc. include E-Z FLEX.