Flexable Systems, Inc.
Country not established
- Devices
- 1
What Flexable Systems, Inc. makes
Flexable Systems, Inc. manufactures the TREMOROMETER, a medical device used for measuring tremors.
The TREMOROMETER is classified as a Class II device and is listed in the FDA 510(k) registry. Flexable Systems, Inc. is based in the US.
Catalogue
Tremorometer Ref K010270
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flexable Systems, Inc. have in the registry?
The registry currently lists 1 device for Flexable Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flexable Systems, Inc.'s devices?
Among its 1 most recently registered device, Flexable Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Flexable Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Flexable Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flexable Systems, Inc. in the registry?
The most recently registered devices listed for Flexable Systems, Inc. include TREMOROMETER.