Medical Device Manufacturer · GB , Birmingham

The Binding Site Group

1 submissions · 1 cleared · Since 2017
1
Total
1
Cleared
0
Denied

The Binding Site Group — FDA 510(k) Submissions

The Binding Site Group has submitted 1 FDA 510(k) premarket notifications since 2017, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, C-reactive Protein . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Immunology 1