Medical Device Manufacturer · IE , Galway

Rockfield Medical

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied

Rockfield Medical — FDA 510(k) Submissions

Rockfield Medical has submitted 2 FDA 510(k) premarket notifications since 2022, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Gastrointestinal Tubes With Enteral Specific Connectors . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Gastroenterology & Urology 2