Veritech, Inc.
Country not established
- Devices
- 1
What Veritech, Inc. makes
Veritech, Inc. manufactures the CHECK-MATE and CHECK-MATE [+] devices, which appear to be Class I medical devices designed for specific diagnostic or monitoring purposes in a clinical setting.
These devices are regulated under the FDA’s 510(k) pathway as Class I products and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Check-Mate And Check-Mate [+] Ref K871359
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Veritech, Inc. have in the registry?
The registry currently lists 1 device for Veritech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Veritech, Inc.'s devices?
Among its 1 most recently registered device, Veritech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Veritech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Veritech, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Veritech, Inc. in the registry?
The most recently registered devices listed for Veritech, Inc. include CHECK-MATE AND CHECK-MATE [+].