Fas Medical, Ltd.
Country not established
- Devices
- 2
What Fas Medical, Ltd. makes
Fas Medical, Ltd. manufactures endoluminal brushes designed for diagnostic or therapeutic procedures within body cavities or ducts, such as the biliary or respiratory systems. These devices are intended for sampling or cleaning internal surfaces during medical interventions.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices. The devices are listed in the FDA’s 510(k) registry and are based in the United States.
Catalogue
Fas Endoluminal Brush Ref K993614
Regimes: 510(k) Registry: 510(k)Fas Endoluminal Brush Ref K012641
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fas Medical, Ltd. have in the registry?
The registry currently lists 2 devices for Fas Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fas Medical, Ltd.'s devices?
Among its 2 most recently registered devices, Fas Medical, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Fas Medical, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fas Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fas Medical, Ltd. in the registry?
The most recently registered devices listed for Fas Medical, Ltd. include FAS ENDOLUMINAL BRUSH.