Signet Radiology, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Signet Radiology, Inc. makes
Signet Radiology, Inc. makes the SIGNET DXIS Direct X-Ray Imaging System, a device used for direct digital radiography in medical imaging.
The SIGNET DXIS Direct X-Ray Imaging System 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
Signet Dxis Direct X-Ray Imaging System Ref K983283
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Signet Radiology, Inc. have in the registry?
The registry currently lists 1 device for Signet Radiology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Signet Radiology, Inc.'s devices?
Among its 1 most recently registered device, Signet Radiology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Signet Radiology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Signet Radiology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Signet Radiology, Inc. in the registry?
The most recently registered devices listed for Signet Radiology, Inc. include SIGNET DXIS DIRECT X-RAY IMAGING SYSTEM.