Procise Diagnostics
Country not established
- Devices
- 1
What Procise Diagnostics makes
Procise Diagnostics manufactures the Procise CRP, a point-of-care diagnostic analyzer, and its associated ProciseDx Calibration Cartridges. These devices are designed for rapid measurement of C-reactive protein (CRP) levels, supporting acute-phase protein monitoring in clinical settings.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Procise Diagnostics have in the registry?
The registry currently lists 1 device for Procise Diagnostics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Procise Diagnostics's devices?
Among its 1 most recently registered device, Procise Diagnostics has devices listed in FDA 510(k) (1 device).
What risk classes do Procise Diagnostics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Procise Diagnostics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Procise Diagnostics in the registry?
The most recently registered devices listed for Procise Diagnostics include Procise CRP, ProciseDx Analyzer, ProciseDx Calibration Cartridge.