Amertek
Country not established
- Devices
- 2
What Amertek makes
Amertek manufactures blood pressure monitors, including the Cardio-Life Model 8823, designed for clinical and home use to measure and display systolic and diastolic blood pressure readings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. Amertek is based in the United States.
Catalogue
Blood Pressure Monitor Ref K812936
Regimes: 510(k) Registry: 510(k)Cardi-O-Life Model 8823 Ref K821090
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amertek have in the registry?
The registry currently lists 2 devices for Amertek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amertek's devices?
Among its 2 most recently registered devices, Amertek has devices listed in FDA 510(k) (2 devices).
What risk classes do Amertek's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Amertek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amertek in the registry?
The most recently registered devices listed for Amertek include BLOOD PRESSURE MONITOR and CARDI-O-LIFE MODEL 8823.