Precision Vascular
Country not established
- Devices
- 1
What Precision Vascular makes
Precision Vascular manufactures the PVS PIVOT steerable microcatheter, designed for vascular access and delivery in interventional procedures.
The company’s products fall under FDA Class II regulation and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Vascular have in the registry?
The registry currently lists 1 device for Precision Vascular. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Vascular's devices?
Among its 1 most recently registered device, Precision Vascular has devices listed in FDA 510(k) (1 device).
What risk classes do Precision Vascular's devices fall under?
Among its 1 most recently registered device, the classes recorded for Precision Vascular's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precision Vascular in the registry?
The most recently registered devices listed for Precision Vascular include PVS PIVOT STEERABLE DELIVERY SYSTEM MICROCATHETER.