Vitatek
Country not established
- Devices
- 2
What Vitatek makes
Vitatek manufactures physiological monitoring devices, including the 500 Monitor Series and the Squinn Vitatek 500 Series Physiological Monitor. These products are designed for real-time patient monitoring, capturing vital signs such as heart rate, blood pressure, and respiratory data.
The company’s portfolio is classified under FDA Class II devices and is regulated through 510(k) clearance in the United States. The devices are listed in the FDA’s 510(k) premarket notification database.
Catalogue
The 500 Monitor Series Ref K823052
510(k) 510(k)Squinn Vitatek 500 Series Physiol. Moni Ref K810755
510(k) 510(k)
Frequently asked questions
How many devices does Vitatek have in the registry?
The registry currently lists 2 devices for Vitatek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitatek's devices?
Among its 2 most recently registered devices, Vitatek has devices listed in FDA 510(k) (2 devices).
What risk classes do Vitatek's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vitatek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitatek in the registry?
The most recently registered devices listed for Vitatek include THE 500 MONITOR SERIES and SQUINN VITATEK 500 SERIES PHYSIOL. MONI.