Endovascular Instruments, Inc.
Country not established
- Devices
- 1
What Endovascular Instruments, Inc. makes
Endovascular Instruments, Inc. manufactures peripheral vascular dilators, which are used to widen narrowed or blocked blood vessels in the legs and lower body to improve blood flow.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Peripheral Vascular Dilator Ref K974617
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endovascular Instruments, Inc. have in the registry?
The registry currently lists 1 device for Endovascular Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endovascular Instruments, Inc.'s devices?
Among its 1 most recently registered device, Endovascular Instruments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Endovascular Instruments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endovascular Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endovascular Instruments, Inc. in the registry?
The most recently registered devices listed for Endovascular Instruments, Inc. include PERIPHERAL VASCULAR DILATOR.