Precisionos Technology, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Precisionos Technology, Inc. makes
Precisionos Technology, Inc. manufactures inVisionOS, which is a medical software device.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
inVisionOS Ref K210344
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precisionos Technology, Inc. have in the registry?
The registry currently lists 1 device for Precisionos Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precisionos Technology, Inc.'s devices?
Among its 1 most recently registered device, Precisionos Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Precisionos Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Precisionos Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precisionos Technology, Inc. in the registry?
The most recently registered devices listed for Precisionos Technology, Inc. include inVisionOS.