Kardiosis Ltd. Co.
Country not established
- Devices
- 1
What Kardiosis Ltd. Co. makes
Kardiosis Ltd. Co. manufactures the ARS-EKG 12K Interpretive Electrocardiography System, a device designed for interpreting 12-lead electrocardiograms to assist in cardiac diagnostics.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed in the 510(k) clearance registry. Kardiosis Ltd. Co. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kardiosis Ltd. Co. have in the registry?
The registry currently lists 1 device for Kardiosis Ltd. Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kardiosis Ltd. Co.'s devices?
Among its 1 most recently registered device, Kardiosis Ltd. Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Kardiosis Ltd. Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kardiosis Ltd. Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kardiosis Ltd. Co. in the registry?
The most recently registered devices listed for Kardiosis Ltd. Co. include ARS-EKG 12K INTERPRETIVE ELECTROCARDIOGRAPHY SYST.