Gamma Medica
Country not established
- Devices
- 1
What Gamma Medica makes
Gamma Medica designs and manufactures the Lumagem scintillation camera, a device used for imaging gamma-emitting radiopharmaceuticals in nuclear medicine procedures.
The company’s portfolio is regulated under FDA’s Class I device classification, with the Lumagem camera listed via the 510(k) pathway. Gamma Medica operates from the United States.
Catalogue
Lumagem Scintillation Camera Ref K993813
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gamma Medica have in the registry?
The registry currently lists 1 device for Gamma Medica. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gamma Medica's devices?
Among its 1 most recently registered device, Gamma Medica has devices listed in FDA 510(k) (1 device).
What risk classes do Gamma Medica's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gamma Medica's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gamma Medica in the registry?
The most recently registered devices listed for Gamma Medica include LUMAGEM SCINTILLATION CAMERA.