Haynes Radiation Ltd., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Haynes Radiation Ltd., Inc. makes
Haynes Radiation Ltd., Inc. manufactures medical radiation simulation and verification systems, including the SIMRITE system for dose verification and the RAD II simulator for training and procedural rehearsal in radiation therapy environments.
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
Simrite Verification And Simulation System Ref K885081
Regimes: 510(k) Registry: 510(k)Rad Ii Simulator Ref K834281
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Haynes Radiation Ltd., Inc. have in the registry?
The registry currently lists 2 devices for Haynes Radiation Ltd., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Haynes Radiation Ltd., Inc.'s devices?
Among its 2 most recently registered devices, Haynes Radiation Ltd., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Haynes Radiation Ltd., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Haynes Radiation Ltd., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Haynes Radiation Ltd., Inc. in the registry?
The most recently registered devices listed for Haynes Radiation Ltd., Inc. include SIMRITE VERIFICATION AND SIMULATION SYSTEM and RAD II SIMULATOR.