Polyval, Inc.
Country not established
- Devices
- 1
What Polyval, Inc. makes
Polyval, Inc. manufactures the Samuels Micro-Scler Catheter, a device used for sclerotherapy procedures to treat vascular conditions by injecting sclerosing agents into small veins.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The products are listed in the FDA’s 510(k) registry. Polyval, Inc. is based in the United States.
Catalogue
Samuels - Micro -Scler Catheter Ref K891164
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Polyval, Inc. have in the registry?
The registry currently lists 1 device for Polyval, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Polyval, Inc.'s devices?
Among its 1 most recently registered device, Polyval, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Polyval, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Polyval, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Polyval, Inc. in the registry?
The most recently registered devices listed for Polyval, Inc. include SAMUELS - MICRO -SCLER CATHETER.