Penrith Corporation
Country not established
- Devices
- 1
What Penrith Corporation makes
Penrith Corporation manufactures the Penrith Elettra Ultrasound System, a diagnostic imaging device designed for real-time ultrasound visualization used in medical diagnostics.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Penrith Elettra Ultrasound System Ref K100598
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Penrith Corporation have in the registry?
The registry currently lists 1 device for Penrith Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Penrith Corporation's devices?
Among its 1 most recently registered device, Penrith Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Penrith Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Penrith Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Penrith Corporation in the registry?
The most recently registered devices listed for Penrith Corporation include PENRITH ELETTRA ULTRASOUND SYSTEM.