Mivi, LLC
Country not established
- Devices
- 1
What Mivi, LLC makes
Mivi, LLC manufactures the MIVI 6F Guide Catheter, a diagnostic and interventional tool used in vascular procedures to facilitate the insertion and navigation of guidewires and other catheters within blood vessels.
The company’s portfolio is regulated under FDA Class II devices, with the MIVI 6F Guide Catheter authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. Mivi, LLC is based in the United States.
Catalogue
Mivi 6F Guide Catheter Ref K140557
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mivi, LLC have in the registry?
The registry currently lists 1 device for Mivi, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mivi, LLC's devices?
Among its 1 most recently registered device, Mivi, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Mivi, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mivi, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mivi, LLC in the registry?
The most recently registered devices listed for Mivi, LLC include MIVI 6F GUIDE CATHETER.