Celtech
Country not established
- Devices
- 1
What Celtech makes
Celtech manufactures the Mitral Valve Orifice Sizer, a diagnostic device used to measure the effective orifice area of the mitral valve in patients, aiding in the assessment of mitral stenosis severity.
The device is classified as Class I under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Mitral Valve Orifice Sizer Ref K820887
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Celtech have in the registry?
The registry currently lists 1 device for Celtech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Celtech's devices?
Among its 1 most recently registered device, Celtech has devices listed in FDA 510(k) (1 device).
What risk classes do Celtech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Celtech's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Celtech in the registry?
The most recently registered devices listed for Celtech include MITRAL VALVE ORIFICE SIZER.