Medical Device Manufacturer · IE , Lisnamuck

Abbott Ireland

2 submissions · 2 cleared · Since 2025
2
Total
2
Cleared
0
Denied

Abbott Ireland — FDA 510(k) Submissions

Abbott Ireland has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Azo Dye, Calcium, Hexokinase, Glucose . Use the specialty filter in the sidebar to narrow results.

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