Elective Vascular Intervention Inc. (Evi)
Country not established
- Devices
- 1
What Elective Vascular Intervention Inc. (Evi) makes
Elective Vascular Intervention Inc. manufactures the EVI Sutured-Clip Applier, a device designed for vascular closure during procedures such as catheter insertions.
The company’s portfolio is regulated under FDA Class II devices, with the EVI Sutured-Clip Applier authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Evi Sutured-Clip Applier Ref K971588
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elective Vascular Intervention Inc. (Evi) have in the registry?
The registry currently lists 1 device for Elective Vascular Intervention Inc. (Evi). Devices recorded under merged duplicate company entries are counted once.
Which registries list Elective Vascular Intervention Inc. (Evi)'s devices?
Among its 1 most recently registered device, Elective Vascular Intervention Inc. (Evi) has devices listed in FDA 510(k) (1 device).
What risk classes do Elective Vascular Intervention Inc. (Evi)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Elective Vascular Intervention Inc. (Evi)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elective Vascular Intervention Inc. (Evi) in the registry?
The most recently registered devices listed for Elective Vascular Intervention Inc. (Evi) include EVI SUTURED-CLIP APPLIER.