Boston Scientific Corporation Northwest Technology
United StatesFDA applicant, unverified
- Devices
- 2
What Boston Scientific Corporation Northwest Technology makes
Boston Scientific Corporation Northwest Technology makes the WireClip Torquer and the Rotablator Rotational Angioplasty System with the Rotalink Exchangeable Catheter.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Wireclip Torquer Ref K003398
Regimes: CE MDR 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Boston Scientific Corporation Northwest Technology have in the registry?
The registry currently lists 2 devices for Boston Scientific Corporation Northwest Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Boston Scientific Corporation Northwest Technology's devices?
Among its 2 most recently registered devices, Boston Scientific Corporation Northwest Technology has devices listed in FDA 510(k) (2 devices).
What risk classes do Boston Scientific Corporation Northwest Technology's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Boston Scientific Corporation Northwest Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Boston Scientific Corporation Northwest Technology in the registry?
The most recently registered devices listed for Boston Scientific Corporation Northwest Technology include WIRECLIP TORQUER and ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM WITH THE ROTALINK EXCHANGEABLE CATHETER.