Cardiovia, Ltd.
IsraelFDA applicant, unverified FDA FEI 3017689643
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
ViaOne Epicardial Access System Ref K243928
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3017689643
- Address
- 13 Wadi El Hadj St., Nazareth Northern
Frequently asked questions
How many devices does Cardiovia, Ltd. have in the registry?
The registry currently lists 1 device for Cardiovia, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiovia, Ltd.'s devices?
Among its 1 most recently registered device, Cardiovia, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiovia, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiovia, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiovia, Ltd. in the registry?
The most recently registered devices listed for Cardiovia, Ltd. include ViaOne Epicardial Access System.