Albert K. Chin
Country not established
- Devices
- 1
What Albert K. Chin makes
Albert K. Chin manufactures a prosthetic cement remover, a surgical instrument designed for the removal of bone cement from prosthetic joints during revision surgeries.
The prosthetic cement remover is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Prosthetic Cement Remover Ref K890285
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Albert K. Chin have in the registry?
The registry currently lists 1 device for Albert K. Chin. Devices recorded under merged duplicate company entries are counted once.
Which registries list Albert K. Chin's devices?
Among its 1 most recently registered device, Albert K. Chin has devices listed in FDA 510(k) (1 device).
What risk classes do Albert K. Chin's devices fall under?
Among its 1 most recently registered device, the classes recorded for Albert K. Chin's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Albert K. Chin in the registry?
The most recently registered devices listed for Albert K. Chin include PROSTHETIC CEMENT REMOVER.