Catheter Sciences Co.
Country not established
- Devices
- 2
What Catheter Sciences Co. makes
Catheter Sciences Co. manufactures diagnostic and therapeutic catheters, including the ECHOMARK PTA ultrasonically located balloon catheter for peripheral vascular interventions and the ECHOMARK CSI interface for imaging guidance systems.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Echomark Csi Interface Ref K910965
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Catheter Sciences Co. have in the registry?
The registry currently lists 2 devices for Catheter Sciences Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Catheter Sciences Co.'s devices?
Among its 2 most recently registered devices, Catheter Sciences Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do Catheter Sciences Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Catheter Sciences Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Catheter Sciences Co. in the registry?
The most recently registered devices listed for Catheter Sciences Co. include ECHOMARK PTA ULTRASONICALLY LOCATED BALLOON CATH. and ECHOMARK CSI INTERFACE.