Multimodal Imaging Services Corporation (Dba Healthlytix)
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- Devices
- 1
What Multimodal Imaging Services Corporation (Dba Healthlytix) makes
Multimodal Imaging Services Corporation (Dba Healthlytix) makes the RSI-MRI+ device, which is a medical imaging system designed for diagnostic use.
The RSI-MRI+ is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Rsi-Mri+ Ref K191278
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Multimodal Imaging Services Corporation (Dba Healthlytix) have in the registry?
The registry currently lists 1 device for Multimodal Imaging Services Corporation (Dba Healthlytix). Devices recorded under merged duplicate company entries are counted once.
Which registries list Multimodal Imaging Services Corporation (Dba Healthlytix)'s devices?
Among its 1 most recently registered device, Multimodal Imaging Services Corporation (Dba Healthlytix) has devices listed in FDA 510(k) (1 device).
What risk classes do Multimodal Imaging Services Corporation (Dba Healthlytix)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Multimodal Imaging Services Corporation (Dba Healthlytix)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Multimodal Imaging Services Corporation (Dba Healthlytix) in the registry?
The most recently registered devices listed for Multimodal Imaging Services Corporation (Dba Healthlytix) include RSI-MRI+.