Diversified P.A.
Country not established
- Devices
- 2
What Diversified P.A. makes
Diversified P.A. manufactures the Xenamatic Series of xenon rebreathing devices, designed for medical anesthesia applications, and the Vidicam 200, a video laryngoscope used for airway visualization during procedures.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Xenamatic Series Of Xenon Rebreath Dev Ref K820571
Regimes: 510(k) Registry: 510(k)Vidicam 200 Ref K812613
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diversified P.A. have in the registry?
The registry currently lists 2 devices for Diversified P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diversified P.A.'s devices?
Among its 2 most recently registered devices, Diversified P.A. has devices listed in FDA 510(k) (2 devices).
What risk classes do Diversified P.A.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Diversified P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diversified P.A. in the registry?
The most recently registered devices listed for Diversified P.A. include XENAMATIC SERIES OF XENON REBREATH DEV and VIDICAM 200.