Ide Vision, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Ide Vision, Ltd. makes
Ide Vision, Ltd. manufactures the MedicCO2LON, a device designed for monitoring and managing carbon dioxide levels in medical settings, likely for use in critical care or respiratory support applications.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
MedicCO2LON (MedicCO2LON) Ref K240847
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ide Vision, Ltd. have in the registry?
The registry currently lists 1 device for Ide Vision, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ide Vision, Ltd.'s devices?
Among its 1 most recently registered device, Ide Vision, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ide Vision, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ide Vision, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ide Vision, Ltd. in the registry?
The most recently registered devices listed for Ide Vision, Ltd. include MedicCO2LON (MedicCO2LON).