Xmar Corp.
Country not established
- Devices
- 1
What Xmar Corp. makes
Xmar Corp. manufactures the PROGNOST ES (Model 0302 0000), a diagnostic device designed for prognostic assessments in clinical settings. This product appears to support predictive analytics for patient outcomes, likely within specialized medical fields such as cardiology or neurology.
The PROGNOST ES is classified as a Class II medical device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States, where its devices are listed for commercial distribution and use.
Catalogue
Prognost Es, Model 0302 0000 Ref K011290
510(k) 510(k)
Frequently asked questions
How many devices does Xmar Corp. have in the registry?
The registry currently lists 1 device for Xmar Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xmar Corp.'s devices?
Among its 1 most recently registered device, Xmar Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Xmar Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Xmar Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xmar Corp. in the registry?
The most recently registered devices listed for Xmar Corp. include PROGNOST ES, MODEL 0302 0000.