Sensocor
Country not established
- Devices
- 1
What Sensocor makes
Sensocor manufactures the Sensocor™ R-Test 24OXL, a device designed for respiratory gas analysis, specifically measuring oxygen and carbon dioxide levels in exhaled breath over a 24-hour period.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The device is listed in the FDA’s 510(k) registry. Sensocor is based in the US.
Catalogue
Sensocor Tm R-Test 24OXL Ref K894234
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sensocor have in the registry?
The registry currently lists 1 device for Sensocor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sensocor's devices?
Among its 1 most recently registered device, Sensocor has devices listed in FDA 510(k) (1 device).
What risk classes do Sensocor's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sensocor's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sensocor in the registry?
The most recently registered devices listed for Sensocor include SENSOCOR TM R-TEST 24OXL.