Js Vascular, Inc.
Country not established
- Devices
- 1
What Js Vascular, Inc. makes
Js Vascular, Inc. manufactures the JS Vascular Guide Wire Vise/Torque Device, a tool designed for securing and manipulating guidewires during vascular procedures.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Js Vascular Guide Wire Vise/Torque Device Ref K032411
510(k) 510(k)
Frequently asked questions
How many devices does Js Vascular, Inc. have in the registry?
The registry currently lists 1 device for Js Vascular, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Js Vascular, Inc.'s devices?
Among its 1 most recently registered device, Js Vascular, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Js Vascular, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Js Vascular, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Js Vascular, Inc. in the registry?
The most recently registered devices listed for Js Vascular, Inc. include JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE.