Traverse Vascular, Inc.
Country not established
- Devices
- 1
What Traverse Vascular, Inc. makes
Traverse Vascular, Inc. manufactures the QuikPass Catheter, a device designed for vascular access procedures, including peripheral and central venous catheterization.
The QuikPass Catheter is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
QuikPass Catheter Ref K214106
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Traverse Vascular, Inc. have in the registry?
The registry currently lists 1 device for Traverse Vascular, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Traverse Vascular, Inc.'s devices?
Among its 1 most recently registered device, Traverse Vascular, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Traverse Vascular, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Traverse Vascular, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Traverse Vascular, Inc. in the registry?
The most recently registered devices listed for Traverse Vascular, Inc. include QuikPass Catheter.