Cardiowise, Inc.
United Statesfrom the FDA registration address FDA FEI 3017991646
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
SQuEEZ Software Ref K201250
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3017991646
- Address
- 535 W. Research Center Blvd., Suite 135, Fayetteville, AR, 72701
Frequently asked questions
How many devices does Cardiowise, Inc. have in the registry?
The registry currently lists 1 device for Cardiowise, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiowise, Inc.'s devices?
Among its 1 most recently registered device, Cardiowise, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiowise, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiowise, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiowise, Inc. in the registry?
The most recently registered devices listed for Cardiowise, Inc. include SQuEEZ Software.