Isodose Control B.V.
NetherlandsFDA applicant, unverified
- Devices
- 4
What Isodose Control B.V. makes
Isodose Control B.V. makes brachytherapy treatment planning systems, including the Flexiplan Brachytherapy Treatment Planning System, Flexiplan 3D and 3D+, and Flexitron. The company also manufactures applicators for afterloading brachytherapy.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Flexitron Ref K070574
Regimes: 510(k) Registry: 510(k)Flexiplan 3D And 3D+ Ref K091145
Regimes: 510(k) Registry: 510(k)Applicators For Afterloading Brachytherapy Ref K082530
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Isodose Control B.V. have in the registry?
The registry currently lists 4 devices for Isodose Control B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Isodose Control B.V.'s devices?
Among its 4 most recently registered devices, Isodose Control B.V. has devices listed in FDA 510(k) (4 devices).
What risk classes do Isodose Control B.V.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Isodose Control B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Isodose Control B.V. in the registry?
The most recently registered devices listed for Isodose Control B.V. include FLEXIPLAN BRACHYTHERAPY TREATMENT PLANNING SYSTEM, FLEXITRON, FLEXIPLAN 3D AND 3D+ and APPLICATORS FOR AFTERLOADING BRACHYTHERAPY.