Intercure, Ltd.
Country not established
- Devices
- 2
What Intercure, Ltd. makes
Intercure, Ltd. manufactures the Respi-Low and the Resperate Model RR-150, which are medical devices designed for respiratory therapy.
These products are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Intercure Ltd. Respi-Low Ref K000405
Regimes: 510(k) Registry: 510(k)Resperate; Model Rr-150 Ref K020399
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intercure, Ltd. have in the registry?
The registry currently lists 2 devices for Intercure, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intercure, Ltd.'s devices?
Among its 2 most recently registered devices, Intercure, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Intercure, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Intercure, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intercure, Ltd. in the registry?
The most recently registered devices listed for Intercure, Ltd. include INTERCURE LTD. RESPI-LOW and RESPERATE; MODEL RR-150.