Medical Device Manufacturer · US , Crofton , MD

Astron Clinica Limited

3 submissions · 3 cleared · Since 2002
3
Total
3
Cleared
0
Denied

Astron Clinica Limited — FDA 510(k) Submissions

Astron Clinica Limited has submitted 3 FDA 510(k) premarket notifications since 2002, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Light Based Imaging . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
Filter by Specialty
All3 General & Plastic Surgery 3