Mediseb, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Mediseb, Ltd. makes
Mediseb, Ltd. manufactures ELFCARE devices, including models 314A through 314G, which are designed for specific low-frequency therapeutic applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Elfcare Device, Models 314A Through 314g Ref K023231
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediseb, Ltd. have in the registry?
The registry currently lists 1 device for Mediseb, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediseb, Ltd.'s devices?
Among its 1 most recently registered device, Mediseb, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mediseb, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mediseb, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mediseb, Ltd. in the registry?
The most recently registered devices listed for Mediseb, Ltd. include ELFCARE DEVICE, MODELS 314A THROUGH 314G.