Medical Device Manufacturer · US , Brea , CA

Clinical Data

1 submissions · 1 cleared · Since 2003
1
Total
1
Cleared
0
Denied

Clinical Data — FDA 510(k) Submissions

Clinical Data has submitted 1 FDA 510(k) premarket notifications since 2003, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Photometric Method, Iron (non-heme) . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
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