Emi Therapy Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Emi Therapy Systems, Inc. makes
Emi Therapy Systems, Inc. manufactures medical linear accelerators and associated planning and treatment systems for radiotherapy, including the EMI Therapy Simulator for treatment preparation and the EMI Four and Therapax 150A accelerators for delivering external beam radiation.
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
System, Planning, Treatment Ref K780948
Regimes: 510(k) Registry: 510(k)Emi Therapy Simulator Ref K771817
Regimes: 510(k) Registry: 510(k)Accelerator, Linear, Med. Ref K780027
Regimes: 510(k) Registry: 510(k)Emi Four Ref K771902
Regimes: 510(k) Registry: 510(k)Therapax 150A Ref K781084
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emi Therapy Systems, Inc. have in the registry?
The registry currently lists 5 devices for Emi Therapy Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emi Therapy Systems, Inc.'s devices?
Among its 5 most recently registered devices, Emi Therapy Systems, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Emi Therapy Systems, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Emi Therapy Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emi Therapy Systems, Inc. in the registry?
The most recently registered devices listed for Emi Therapy Systems, Inc. include SYSTEM, PLANNING, TREATMENT, EMI THERAPY SIMULATOR, ACCELERATOR, LINEAR, MED. and EMI FOUR.