Cardioset Medical, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Cardioset Medical, Ltd. makes
Cardioset Medical, Ltd. manufactures the Edema Guard Monitor (EGM), a device designed to monitor and assess fluid accumulation in patients, particularly for detecting edema.
The Edema Guard Monitor is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Edema Guard Monitor (EGM) CardioSet-001 Ref K250922
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardioset Medical, Ltd. have in the registry?
The registry currently lists 1 device for Cardioset Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardioset Medical, Ltd.'s devices?
Among its 1 most recently registered device, Cardioset Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardioset Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardioset Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardioset Medical, Ltd. in the registry?
The most recently registered devices listed for Cardioset Medical, Ltd. include Edema Guard Monitor (EGM) CardioSet-001.