Johnson & Johnson Interventional Systems
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Palmaz Biliary Stent Ref K905720
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Johnson & Johnson Interventional Systems have in the registry?
The registry currently lists 2 devices for Johnson & Johnson Interventional Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Johnson & Johnson Interventional Systems's devices?
Among its 2 most recently registered devices, Johnson & Johnson Interventional Systems has devices listed in FDA 510(k) (2 devices).
What risk classes do Johnson & Johnson Interventional Systems's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Johnson & Johnson Interventional Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Johnson & Johnson Interventional Systems in the registry?
The most recently registered devices listed for Johnson & Johnson Interventional Systems include PALMAZ(TM) BALLOON-EXPANDABLE STENT, MODIFICATION and PALMAZ BILIARY STENT.