Diatech Diagnostics, Inc.
Country not established
- Devices
- 1
What Diatech Diagnostics, Inc. makes
Diatech Diagnostics, Inc. manufactures the URISCREEN, a diagnostic device used for detecting and identifying urinary tract infections by analyzing urine samples for bacterial presence and species identification.
The URISCREEN is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Uriscreen Ref K981084
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diatech Diagnostics, Inc. have in the registry?
The registry currently lists 1 device for Diatech Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diatech Diagnostics, Inc.'s devices?
Among its 1 most recently registered device, Diatech Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Diatech Diagnostics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Diatech Diagnostics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Diatech Diagnostics, Inc. in the registry?
The most recently registered devices listed for Diatech Diagnostics, Inc. include URISCREEN.