Ventripoint, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
VentriPoint Medical System Ref K150628
Regimes: 510(k) Registry: 510(k)Ventripoint Medical System Ref K140153
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ventripoint, Inc. have in the registry?
The registry currently lists 2 devices for Ventripoint, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ventripoint, Inc.'s devices?
Among its 2 most recently registered devices, Ventripoint, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ventripoint, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ventripoint, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ventripoint, Inc. in the registry?
The most recently registered devices listed for Ventripoint, Inc. include VentriPoint Medical System.