Cibernet Systems Corp.
Country not established
- Devices
- 1
What Cibernet Systems Corp. makes
Cibernet Systems Corp. manufactures the MEDSTAR series of devices, including models 220, 230, 360, and 370, which are identified by model numbers 533-220, 533-230, 533-360, and 533-370 respectively.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cibernet Systems Corp. have in the registry?
The registry currently lists 1 device for Cibernet Systems Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cibernet Systems Corp.'s devices?
Among its 1 most recently registered device, Cibernet Systems Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Cibernet Systems Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cibernet Systems Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cibernet Systems Corp. in the registry?
The most recently registered devices listed for Cibernet Systems Corp. include MEDSTAR 220, MODEL 533-220; MEDSTAR 230, MODEL 533-230; MEDSTAR 360, MODEL 533-360; MEDSTAR 370, MODEL 533-370.