MicroVention, Inc., d/b/a Terumo Neuro
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
ISAAC Neurovascular Navigation Catheter Ref K261808
Regimes: 510(k) Registry: 510(k)BOBBY Balloon Guide Catheter Ref K261549
Regimes: 510(k) Registry: 510(k)Mayumi™ Thrombectomy System Ref K254035
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does MicroVention, Inc., d/b/a Terumo Neuro have in the registry?
The registry currently lists 3 devices for MicroVention, Inc., d/b/a Terumo Neuro. Devices recorded under merged duplicate company entries are counted once.
Which registries list MicroVention, Inc., d/b/a Terumo Neuro's devices?
Among its 3 most recently registered devices, MicroVention, Inc., d/b/a Terumo Neuro has devices listed in FDA 510(k) (3 devices).
What risk classes do MicroVention, Inc., d/b/a Terumo Neuro's devices fall under?
Among its 3 most recently registered devices, the classes recorded for MicroVention, Inc., d/b/a Terumo Neuro's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MicroVention, Inc., d/b/a Terumo Neuro in the registry?
The most recently registered devices listed for MicroVention, Inc., d/b/a Terumo Neuro include ISAAC Neurovascular Navigation Catheter, BOBBY Balloon Guide Catheter and Mayumi™ Thrombectomy System.