Ansys, Inc.
Country not established
- Devices
- 1
What Ansys, Inc. makes
Ansys, Inc. manufactures the ON.SITE ALCOHOL device.
This product is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
On.site Alcohol Ref K963197
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ansys, Inc. have in the registry?
The registry currently lists 1 device for Ansys, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ansys, Inc.'s devices?
Among its 1 most recently registered device, Ansys, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ansys, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ansys, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ansys, Inc. in the registry?
The most recently registered devices listed for Ansys, Inc. include ON.SITE ALCOHOL.