Truevision Instruments
Country not established
- Devices
- 1
What Truevision Instruments makes
Truevision Instruments manufactures the TGDC-01 PRA, a device designed for retinal imaging and diagnostic purposes, enabling detailed visualization of the posterior retina.
The TGDC-01 PRA is classified as a Class II medical device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Tgdc-01 Pra Ref K021937
510(k) 510(k)
Frequently asked questions
How many devices does Truevision Instruments have in the registry?
The registry currently lists 1 device for Truevision Instruments. Devices recorded under merged duplicate company entries are counted once.
Which registries list Truevision Instruments's devices?
Among its 1 most recently registered device, Truevision Instruments has devices listed in FDA 510(k) (1 device).
What risk classes do Truevision Instruments's devices fall under?
Among its 1 most recently registered device, the classes recorded for Truevision Instruments's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Truevision Instruments in the registry?
The most recently registered devices listed for Truevision Instruments include TGDC-01 PRA.