Neuro Vasx, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Neuro Vasx, Inc. makes
Neuro Vasx, Inc. makes infusion catheters, specifically the NeuroEdge Infusion Catheter and the NeuroVasx Sub-Microinfusion Catheter, which are designed for delivering fluids or medications within the neurovascular system.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Neuroedge Infusion Catheter Ref K011646
Regimes: 510(k) Registry: 510(k)Neurovasx Sub-Microinfusion Catheter Ref K984258
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuro Vasx, Inc. have in the registry?
The registry currently lists 2 devices for Neuro Vasx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuro Vasx, Inc.'s devices?
Among its 2 most recently registered devices, Neuro Vasx, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Neuro Vasx, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neuro Vasx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuro Vasx, Inc. in the registry?
The most recently registered devices listed for Neuro Vasx, Inc. include NEUROEDGE INFUSION CATHETER and NEUROVASX SUB-MICROINFUSION CATHETER.