Pem Technologies
Country not established
- Devices
- 2
What Pem Technologies makes
Pem Technologies makes the PEM 2400 PET scanner and a portable breast compression device.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Pem 2400 Pet Scanner Ref K032063
Regimes: 510(k) Registry: 510(k)Portable Breast Compression Device Ref K003775
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pem Technologies have in the registry?
The registry currently lists 2 devices for Pem Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pem Technologies's devices?
Among its 2 most recently registered devices, Pem Technologies has devices listed in FDA 510(k) (2 devices).
What risk classes do Pem Technologies's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pem Technologies's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pem Technologies in the registry?
The most recently registered devices listed for Pem Technologies include PEM 2400 PET SCANNER and PORTABLE BREAST COMPRESSION DEVICE.