Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC)
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- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pacific Plus PTA Catheter Ref K202800
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC) have in the registry?
The registry currently lists 1 device for Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC). Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC)'s devices?
Among its 1 most recently registered device, Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC) has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC) in the registry?
The most recently registered devices listed for Medtronic Vascular, Inc(Formerly D.B.A Ev3 Inc., Covidien, LLC) include Pacific Plus PTA Catheter.