Core Healthcare, Ltd.
Country not established
- Devices
- 1
What Core Healthcare, Ltd. makes
Core Healthcare, Ltd. manufactures the CORELIFE, a medical device designed for patient monitoring or support in clinical settings, though specific applications are not detailed.
The CORELIFE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Corelife Ref K964230
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Core Healthcare, Ltd. have in the registry?
The registry currently lists 1 device for Core Healthcare, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Core Healthcare, Ltd.'s devices?
Among its 1 most recently registered device, Core Healthcare, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Core Healthcare, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Core Healthcare, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Core Healthcare, Ltd. in the registry?
The most recently registered devices listed for Core Healthcare, Ltd. include CORELIFE.