Zatek
Country not established
- Devices
- 1
What Zatek makes
Zatek manufactures a pressure monitoring device, specifically the Model 212, designed for measuring and displaying pressure readings in clinical or industrial settings.
The pressure monitor Model 212 falls under FDA Class I regulation and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Pressure Monitor, Model 212 Ref K790302
510(k) 510(k)
Frequently asked questions
How many devices does Zatek have in the registry?
The registry currently lists 1 device for Zatek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zatek's devices?
Among its 1 most recently registered device, Zatek has devices listed in FDA 510(k) (1 device).
What risk classes do Zatek's devices fall under?
Among its 1 most recently registered device, the classes recorded for Zatek's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Zatek in the registry?
The most recently registered devices listed for Zatek include PRESSURE MONITOR, MODEL 212.