Vascon, LLC
United StatesFDA applicant, unverified
- Devices
- 4
What Vascon, LLC makes
Vascon, LLC manufactures specialized catheters, including the VASCON ROAMER MICROCATHETER, the VASCON NEUROPATH GUIDING CATHETER, and the VASCON POLARIS GUIDING CATHETER. These devices are designed for precise navigation and delivery within vascular and neurological procedures.
The company's portfolio is regulated as Class II medical devices and is listed in the FDA 510(k) registry. Vascon, LLC is based in the United States.
Catalogue
Vascon Roamer Microcatheter Ref K053310
Regimes: 510(k) Registry: 510(k)Vascon Neuropath Guiding Catheter Ref K052004
Regimes: 510(k) Registry: 510(k)Vascon Polaris Guiding Catheter Ref K033633
Regimes: 510(k) Registry: 510(k)Vascon Polaris Guiding Catheter Ref K043387
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascon, LLC have in the registry?
The registry currently lists 4 devices for Vascon, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascon, LLC's devices?
Among its 4 most recently registered devices, Vascon, LLC has devices listed in FDA 510(k) (4 devices).
What risk classes do Vascon, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Vascon, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vascon, LLC in the registry?
The most recently registered devices listed for Vascon, LLC include VASCON ROAMER MICROCATHETER, VASCON NEUROPATH GUIDING CATHETER and VASCON POLARIS GUIDING CATHETER.