Medrad Interventional/Possis
Country not established
- Devices
- 2
What Medrad Interventional/Possis makes
Medrad Interventional/Possis manufactures thrombectomy and aspiration devices for vascular interventions, including the AngioJet Solent Proxi Thrombectomy Set and the Fetch 2 Aspiration Catheter. These products are designed for removing blood clots and debris from arteries during endovascular procedures.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Fetch 2 Aspiration Catheter Model 109400-001 Ref K101354
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medrad Interventional/Possis have in the registry?
The registry currently lists 2 devices for Medrad Interventional/Possis. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medrad Interventional/Possis's devices?
Among its 2 most recently registered devices, Medrad Interventional/Possis has devices listed in FDA 510(k) (2 devices).
What risk classes do Medrad Interventional/Possis's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medrad Interventional/Possis's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medrad Interventional/Possis in the registry?
The most recently registered devices listed for Medrad Interventional/Possis include ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001 and FETCH 2 ASPIRATION CATHETER MODEL 109400-001.