Tokyo Boeki Medical System, Ltd.
Country not established
- Devices
- 1
What Tokyo Boeki Medical System, Ltd. makes
Tokyo Boeki Medical System, Ltd. manufactures the Prestige Models 24I and 400, as well as the MGC Model 240, which are intended for medical imaging or diagnostic purposes in radiology settings.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Prestige Models 24I And 400 And Mgc Model 240 Ref K040958
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tokyo Boeki Medical System, Ltd. have in the registry?
The registry currently lists 1 device for Tokyo Boeki Medical System, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tokyo Boeki Medical System, Ltd.'s devices?
Among its 1 most recently registered device, Tokyo Boeki Medical System, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Tokyo Boeki Medical System, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tokyo Boeki Medical System, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tokyo Boeki Medical System, Ltd. in the registry?
The most recently registered devices listed for Tokyo Boeki Medical System, Ltd. include PRESTIGE MODELS 24I AND 400 AND MGC MODEL 240.