Speywood Medical, Ltd.
Country not established
- Devices
- 1
What Speywood Medical, Ltd. makes
Speywood Medical, Ltd. manufactures the C TEC Series 9000 ECG electrodes, which are reusable adhesive electrodes designed for electrocardiogram (ECG) monitoring to record heart electrical activity.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
C Tec Series 9000 E.C.G. Electrode Ref K831977
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Speywood Medical, Ltd. have in the registry?
The registry currently lists 1 device for Speywood Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Speywood Medical, Ltd.'s devices?
Among its 1 most recently registered device, Speywood Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Speywood Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Speywood Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Speywood Medical, Ltd. in the registry?
The most recently registered devices listed for Speywood Medical, Ltd. include C TEC SERIES 9000 E.C.G. ELECTRODE.