Freedom Meditech, Inc.
Country not established
- Devices
- 1
What Freedom Meditech, Inc. makes
Freedom Meditech, Inc. makes the CLEARPATH DS-120(R) LENS FLUORESCENCE BIOMICROSCOPE, a device used for ophthalmic imaging that utilizes fluorescence biomicroscopy to examine the lens of the eye.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Freedom Meditech, Inc. have in the registry?
The registry currently lists 1 device for Freedom Meditech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Freedom Meditech, Inc.'s devices?
Among its 1 most recently registered device, Freedom Meditech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Freedom Meditech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Freedom Meditech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Freedom Meditech, Inc. in the registry?
The most recently registered devices listed for Freedom Meditech, Inc. include CLEARPATH DS-120(R) LENS FLUORESCENCE BIOMICROSCOPE.