Mds Nordion, Inc.
CanadaFDA applicant, unverified
- Devices
- 9
What Mds Nordion, Inc. makes
Mds Nordion, Inc. manufactures the THERATRON EQUINOX, models 80 cm and 100 cm, which are medical devices used for radiation therapy.
The company is based in the US, and its devices are listed in the FDA 510(k) registry as Class II medical devices.
Catalogue
Raycell Ref K032684
Regimes: 510(k) Registry: 510(k)Dcm 2.0 Ref K020971
Regimes: 510(k) Registry: 510(k)Avanza Ref K060870
Regimes: 510(k) Registry: 510(k)Raycell X-Ray Blood Irradiator Ref K051065
Regimes: 510(k) Registry: 510(k)Dcm 1.0 Ref K011246
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Gammacell 1000 Elite And Gammacell 3000 Elan Ref K050963
Regimes: 510(k) Registry: 510(k)Theratron Equinox, Models 80 Cm And 100 Cm Ref K053485
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mds Nordion, Inc. have in the registry?
The registry currently lists 9 devices for Mds Nordion, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mds Nordion, Inc.'s devices?
Among its 9 most recently registered devices, Mds Nordion, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Mds Nordion, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Mds Nordion, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mds Nordion, Inc. in the registry?
The most recently registered devices listed for Mds Nordion, Inc. include RAYCELL, DCM 2.0, AVANZA and RAYCELL X-RAY BLOOD IRRADIATOR.