Cross Vascular, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Cross Vascular, Inc. makes
Cross Vascular, Inc. manufactures radiofrequency (RF) ablation systems, including RF generators and transseptal needles designed for cardiac procedures. The RF generator operates with an optional footswitch accessory, while the transseptal needle and connection cable are used for creating septal defects under RF energy. These devices are intended for interventional cardiology applications.
The company’s portfolio is classified under FDA’s Class II regulatory category and is supported by 510(k) clearance records. The devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Cross Vascular, Inc. have in the registry?
The registry currently lists 2 devices for Cross Vascular, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cross Vascular, Inc.'s devices?
Among its 2 most recently registered devices, Cross Vascular, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cross Vascular, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cross Vascular, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cross Vascular, Inc. in the registry?
The most recently registered devices listed for Cross Vascular, Inc. include Cross Vascular RF Generator and Footswitch (optional accessory) and Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable.