Mrc Systems GmbH
GermanyFDA applicant, unverified
- Devices
- 3
What Mrc Systems GmbH makes
Mrc Systems GmbH manufactures radiation therapy accessories, including the KONRAD system for patient positioning and immobilization, the MODULEAF for leaf positioning in linear accelerators, and the MINI MULTILEAF COLLIMATOR (KMI) for precise beam shaping in radiotherapy treatments.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Konrad, Model V.2.0 Ref K022307
Regimes: 510(k) Registry: 510(k)Moduleaf Ref K030609
Regimes: 510(k) Registry: 510(k)Mini Multileaf Collimator, Model Kmi Ref K011816
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mrc Systems GmbH have in the registry?
The registry currently lists 3 devices for Mrc Systems GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mrc Systems GmbH's devices?
Among its 3 most recently registered devices, Mrc Systems GmbH has devices listed in FDA 510(k) (3 devices).
What risk classes do Mrc Systems GmbH's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mrc Systems GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mrc Systems GmbH in the registry?
The most recently registered devices listed for Mrc Systems GmbH include KONRAD, MODEL V.2.0, MODULEAF and MINI MULTILEAF COLLIMATOR, MODEL KMI.