Marconi Medical Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Boluspro Ultra Ref K002005
Regimes: 510(k) Registry: 510(k)MX8000 Idt Ct System Ref K012009
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Marconi Medical Systems, Inc. have in the registry?
The registry currently lists 2 devices for Marconi Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Marconi Medical Systems, Inc.'s devices?
Among its 2 most recently registered devices, Marconi Medical Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Marconi Medical Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Marconi Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Marconi Medical Systems, Inc. in the registry?
The most recently registered devices listed for Marconi Medical Systems, Inc. include BOLUSPRO ULTRA and MX8000 IDT CT SYSTEM.