Psp Corporation
JapanFDA applicant, unverified
- Devices
- 1
What Psp Corporation makes
Psp Corporation manufactures the EV Insite System, a device designed for electrophysiological mapping and catheter ablation in cardiac procedures, used to visualize and treat arrhythmias.
The EV Insite System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
EV Insite System Ref K152716
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Psp Corporation have in the registry?
The registry currently lists 1 device for Psp Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Psp Corporation's devices?
Among its 1 most recently registered device, Psp Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Psp Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Psp Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Psp Corporation in the registry?
The most recently registered devices listed for Psp Corporation include EV Insite System.