Salutaris Medical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Salutaris Medical Devices, Inc. makes
Salutaris Medical Devices, Inc. manufactures radionuclide brachytherapy sources, including the SMD Sr90-1 and SMD-Sr90-DA models, designed for targeted radiation therapy in medical treatments.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
SMD Sr90-1 Radionuclide Brachytherapy Source Ref K142701
Regimes: 510(k) Registry: 510(k)SMD-Sr90-DA Radionuclide Brachytherapy Source Ref K163206
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Salutaris Medical Devices, Inc. have in the registry?
The registry currently lists 2 devices for Salutaris Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Salutaris Medical Devices, Inc.'s devices?
Among its 2 most recently registered devices, Salutaris Medical Devices, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Salutaris Medical Devices, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Salutaris Medical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Salutaris Medical Devices, Inc. in the registry?
The most recently registered devices listed for Salutaris Medical Devices, Inc. include SMD Sr90-1 Radionuclide Brachytherapy Source and SMD-Sr90-DA Radionuclide Brachytherapy Source.