Endovascular, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Disposable Optical Valvulotome Ref K924075
Regimes: 510(k) Registry: 510(k)Disposable Steerable Angioscope Ref K931421
Regimes: 510(k) Registry: 510(k)Disposable Vascular Angioscope Ref K923996
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endovascular, Inc. have in the registry?
The registry currently lists 3 devices for Endovascular, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endovascular, Inc.'s devices?
Among its 3 most recently registered devices, Endovascular, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Endovascular, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Endovascular, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endovascular, Inc. in the registry?
The most recently registered devices listed for Endovascular, Inc. include DISPOSABLE OPTICAL VALVULOTOME, DISPOSABLE STEERABLE ANGIOSCOPE and DISPOSABLE VASCULAR ANGIOSCOPE.