Medical Device Manufacturer · NO , Oslo

Abbott Diagnostics Technologies AS

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Abbott Diagnostics Technologies AS — FDA 510(k) Submissions

Abbott Diagnostics Technologies AS has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Assay, Glycosylated Hemoglobin . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Chemistry 1