Medical Device Manufacturer · GB , Oxon

Penlon Limited

3 submissions · 3 cleared · Since 2005
3
Total
3
Cleared
0
Denied

Penlon Limited — FDA 510(k) Submissions

Penlon Limited has submitted 3 FDA 510(k) premarket notifications since 2005, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Vaporizer, Anesthesia, Non-heated, Ventilator, Continuous, Facility Use . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
Filter by Specialty
All3 Anesthesiology 3