Matritech, Inc.
Country not established
- Devices
- 1
What Matritech, Inc. makes
Matritech, Inc. manufactures the NMP22 BLADDERCHEK KIT and NMP22 CONTROL KIT, which are medical devices used for bladder cancer detection.
These devices are classified as Class II and are listed in the FDA 510(k) registry. Matritech, Inc. is based in the US.
Catalogue
NMP22 Bladderchek Kit, NMP22 Control Kit Ref K021231
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Matritech, Inc. have in the registry?
The registry currently lists 1 device for Matritech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Matritech, Inc.'s devices?
Among its 1 most recently registered device, Matritech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Matritech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Matritech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Matritech, Inc. in the registry?
The most recently registered devices listed for Matritech, Inc. include NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT.