Medical Device Manufacturer · US , Portola Valley , CA

Albert K. Chin

1 submissions · 1 cleared · Since 1989
1
Total
1
Cleared
0
Denied

Albert K. Chin — FDA 510(k) Submissions

Albert K. Chin has submitted 1 FDA 510(k) premarket notifications since 1989, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Cement Removal Extraction . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Orthopedic 1