Vascular Pathways
Country not established
- Devices
- 4
What Vascular Pathways makes
Vascular Pathways manufactures intravascular catheter systems designed for rapid vascular access, including the RIVS Rapid Intravascular Catheter Start System. These devices are intended for use in procedures requiring quick and reliable vascular entry, such as emergency or critical care interventions.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. The devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Accucath Midline Catheter System Ref K142136
Regimes: 510(k) Registry: 510(k)Accucath Bc Intravascular Catheter System Ref K140504
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascular Pathways have in the registry?
The registry currently lists 4 devices for Vascular Pathways. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascular Pathways's devices?
Among its 4 most recently registered devices, Vascular Pathways has devices listed in FDA 510(k) (4 devices).
What risk classes do Vascular Pathways's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Vascular Pathways's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vascular Pathways in the registry?
The most recently registered devices listed for Vascular Pathways include RAPID INTRAVASCULAR CATHETER START SYSTEM 22 GAUGE / 20 GAUGE / 18 GAUGE, ACCUCATH MIDLINE CATHETER SYSTEM, ACCUCATH BC INTRAVASCULAR CATHETER SYSTEM and VASCULAR PATHWAYS RIVS RAPID INTRAVASCULAR CATHETER START SYSTEM.