Retroperfusion Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Retroperfusion Systems, Inc. makes
Retroperfusion Systems, Inc. manufactures vascular catheters designed for targeted drug delivery and perfusion procedures. Their product line includes the RSI Femoral Guiding Catheter, used for guiding interventions in peripheral vascular access, and the Corday Coronary Sinus Infusion Catheter, intended for localized infusion within the coronary sinus.
These devices are classified under Class II by the FDA and are authorised through the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Rsi Femoral Guiding Catheter Ref K902943
Regimes: 510(k) Registry: 510(k)Corday Coronary Sinus Infusion Catheter Ref K865074
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Retroperfusion Systems, Inc. have in the registry?
The registry currently lists 2 devices for Retroperfusion Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retroperfusion Systems, Inc.'s devices?
Among its 2 most recently registered devices, Retroperfusion Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Retroperfusion Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Retroperfusion Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retroperfusion Systems, Inc. in the registry?
The most recently registered devices listed for Retroperfusion Systems, Inc. include RSI FEMORAL GUIDING CATHETER and CORDAY CORONARY SINUS INFUSION CATHETER.