Regam Medical Systems
CanadaFDA applicant, unverified
- Devices
- 1
What Regam Medical Systems makes
Regam Medical Systems manufactures the SENS-A-RAY, a device designed for monitoring and detecting radiation exposure levels in medical and industrial settings.
The SENS-A-RAY is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Sens-A-Ray Ref K923067
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Regam Medical Systems have in the registry?
The registry currently lists 1 device for Regam Medical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regam Medical Systems's devices?
Among its 1 most recently registered device, Regam Medical Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Regam Medical Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Regam Medical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Regam Medical Systems in the registry?
The most recently registered devices listed for Regam Medical Systems include SENS-A-RAY.