Medical Device Manufacturer · IT , Saluggia

Corcym S.r.l.

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Corcym S.r.l. — FDA 510(k) Submissions

Corcym S.r.l. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ring, Annuloplasty . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Cardiovascular 1