Conway Electronic Enterprises, Ltd.
Country not established
- Devices
- 1
What Conway Electronic Enterprises, Ltd. makes
Conway Electronic Enterprises, Ltd. manufactures the CARDIART 108T/313, a medical device designed for cardiac monitoring and rhythm analysis, likely used in clinical or diagnostic settings to assess heart function.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II device, indicating it is subject to performance-based requirements. The device is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Cardiart 108T/313 Ref K761014
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Conway Electronic Enterprises, Ltd. have in the registry?
The registry currently lists 1 device for Conway Electronic Enterprises, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Conway Electronic Enterprises, Ltd.'s devices?
Among its 1 most recently registered device, Conway Electronic Enterprises, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Conway Electronic Enterprises, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Conway Electronic Enterprises, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Conway Electronic Enterprises, Ltd. in the registry?
The most recently registered devices listed for Conway Electronic Enterprises, Ltd. include CARDIART 108T/313.