Kendall-Ltp
Country not established
- Devices
- 1
What Kendall-Ltp makes
Kendall-Ltp manufactures disposable ECG electrodes, designed for single-use attachment to the skin during electrocardiogram monitoring to capture heart activity signals.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Disposable Ecg Electrode Ref K953649
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kendall-Ltp have in the registry?
The registry currently lists 1 device for Kendall-Ltp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kendall-Ltp's devices?
Among its 1 most recently registered device, Kendall-Ltp has devices listed in FDA 510(k) (1 device).
What risk classes do Kendall-Ltp's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kendall-Ltp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kendall-Ltp in the registry?
The most recently registered devices listed for Kendall-Ltp include DISPOSABLE ECG ELECTRODE.