Carevature Medical, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Carevature Medical, Ltd. makes
Carevature Medical, Ltd. manufactures the DReal, a device designed for real-time diagnostic imaging and monitoring in medical settings, likely targeting specific clinical applications requiring precise data acquisition.
The company’s portfolio is regulated under FDA Class II devices, with the DReal authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
DReal Ref K153519
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Carevature Medical, Ltd. have in the registry?
The registry currently lists 1 device for Carevature Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carevature Medical, Ltd.'s devices?
Among its 1 most recently registered device, Carevature Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Carevature Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Carevature Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Carevature Medical, Ltd. in the registry?
The most recently registered devices listed for Carevature Medical, Ltd. include DReal.