Radiadyne, LLC (Specification Developer)
Country not established
- Devices
- 1
What Radiadyne, LLC (Specification Developer) makes
Radiadyne, LLC designs and develops brachytherapy applicator balloon devices used in radiation oncology for targeted cancer treatment.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Radiapak Brachytherapy Applicator Balloon Device Ref K120344
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radiadyne, LLC (Specification Developer) have in the registry?
The registry currently lists 1 device for Radiadyne, LLC (Specification Developer). Devices recorded under merged duplicate company entries are counted once.
Which registries list Radiadyne, LLC (Specification Developer)'s devices?
Among its 1 most recently registered device, Radiadyne, LLC (Specification Developer) has devices listed in FDA 510(k) (1 device).
What risk classes do Radiadyne, LLC (Specification Developer)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Radiadyne, LLC (Specification Developer)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Radiadyne, LLC (Specification Developer) in the registry?
The most recently registered devices listed for Radiadyne, LLC (Specification Developer) include RADIAPAK BRACHYTHERAPY APPLICATOR BALLOON DEVICE.