D. Jenkins
Country not established
- Devices
- 1
What D. Jenkins makes
D. Jenkins manufactures HEARTWATCH, a cardiac monitoring device designed for continuous or intermittent electrocardiogram (ECG) tracking, typically used in outpatient or home settings to detect arrhythmias or other cardiac irregularities.
The HEARTWATCH device falls under FDA Class II regulation and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Heartwatch Ref K800519
510(k) 510(k)
Frequently asked questions
How many devices does D. Jenkins have in the registry?
The registry currently lists 1 device for D. Jenkins. Devices recorded under merged duplicate company entries are counted once.
Which registries list D. Jenkins's devices?
Among its 1 most recently registered device, D. Jenkins has devices listed in FDA 510(k) (1 device).
What risk classes do D. Jenkins's devices fall under?
Among its 1 most recently registered device, the classes recorded for D. Jenkins's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D. Jenkins in the registry?
The most recently registered devices listed for D. Jenkins include HEARTWATCH.