Polysil, Inc.
Country not established
- Devices
- 1
What Polysil, Inc. makes
Polysil, Inc. manufactures the Folhy Catheter, a medical device designed for specific urological applications, including drainage and irrigation procedures.
The Folhy Catheter is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Folhy Catheter Ref K771860
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Polysil, Inc. have in the registry?
The registry currently lists 1 device for Polysil, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Polysil, Inc.'s devices?
Among its 1 most recently registered device, Polysil, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Polysil, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Polysil, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Polysil, Inc. in the registry?
The most recently registered devices listed for Polysil, Inc. include FOLHY CATHETER.