Fujifilm Meidcal Systems U.S.A., Inc.
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Synapse 3D Tensor Analysis Ref K141514
Regimes: 510(k) Registry: 510(k)Synapse 3D Liver and Kidney Analysis Ref K142521
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fujifilm Meidcal Systems U.S.A., Inc. have in the registry?
The registry currently lists 2 devices for Fujifilm Meidcal Systems U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fujifilm Meidcal Systems U.S.A., Inc.'s devices?
Among its 2 most recently registered devices, Fujifilm Meidcal Systems U.S.A., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Fujifilm Meidcal Systems U.S.A., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fujifilm Meidcal Systems U.S.A., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fujifilm Meidcal Systems U.S.A., Inc. in the registry?
The most recently registered devices listed for Fujifilm Meidcal Systems U.S.A., Inc. include SYNAPSE 3D TENSOR ANALYSIS and Synapse 3D Liver and Kidney Analysis.