Trans Vascular Incorporated
United StatesFDA applicant, unverified
- Devices
- 2
What Trans Vascular Incorporated makes
Trans Vascular Incorporated manufactures the CROSSPOINT TRANSACCESS CATHETER and its variant, the CROSSPOINT TRANSACCESS CATHETER (Model TA-XP-001), designed for vascular access procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Crosspoint Transaccess Catheter Ref K013363
Regimes: 510(k) Registry: 510(k)Crosspoint Transaccess Catheter, Model Ta-Xp-001 Ref K031920
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Trans Vascular Incorporated have in the registry?
The registry currently lists 2 devices for Trans Vascular Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trans Vascular Incorporated's devices?
Among its 2 most recently registered devices, Trans Vascular Incorporated has devices listed in FDA 510(k) (2 devices).
What risk classes do Trans Vascular Incorporated's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Trans Vascular Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trans Vascular Incorporated in the registry?
The most recently registered devices listed for Trans Vascular Incorporated include CROSSPOINT TRANSACCESS CATHETER and CROSSPOINT TRANSACCESS CATHETER, MODEL TA-XP-001.