Vector Corporation, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Vector Corporation, LLC makes
Vector Corporation, LLC manufactures the Vector PTA Balloon Dilatation Catheter, a device used for percutaneous transluminal angioplasty (PTA) to mechanically widen narrowed or obstructed blood vessels, typically in peripheral arteries.
The company’s portfolio is regulated under FDA Class II devices, with the Vector PTA Balloon Dilatation Catheter authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
First Aid Kit(S) Ref K963298
Regimes: 510(k) Registry: 510(k)Vector PTA Balloon Dilatation Catheter Ref K143652
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vector Corporation, LLC have in the registry?
The registry currently lists 2 devices for Vector Corporation, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vector Corporation, LLC's devices?
Among its 2 most recently registered devices, Vector Corporation, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Vector Corporation, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vector Corporation, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vector Corporation, LLC in the registry?
The most recently registered devices listed for Vector Corporation, LLC include FIRST AID KIT(S) and Vector PTA Balloon Dilatation Catheter.