Medical Device Manufacturer · IE , Galway

Phenox Limited

4 submissions · 4 cleared · Since 2019
4
Total
4
Cleared
0
Denied

Phenox Limited — FDA 510(k) Submissions

Phenox Limited has submitted 4 FDA 510(k) premarket notifications since 2019, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment, Wire, Guide, Catheter . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Neurology 4