Automated Screening Devices
Country not established
- Devices
- 2
What Automated Screening Devices makes
The company manufactures automated screening devices, including the SENTRY system and non-invasive blood pressure monitors designed for clinical or point-of-care use.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Sentry Ref K792653
Regimes: 510(k) Registry: 510(k)Monitor, Non-Invasive Blood Pressure Ref K782000
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Automated Screening Devices have in the registry?
The registry currently lists 2 devices for Automated Screening Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Automated Screening Devices's devices?
Among its 2 most recently registered devices, Automated Screening Devices has devices listed in FDA 510(k) (2 devices).
What risk classes do Automated Screening Devices's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Automated Screening Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Automated Screening Devices in the registry?
The most recently registered devices listed for Automated Screening Devices include SENTRY and MONITOR, NON-INVASIVE BLOOD PRESSURE.