Medical Device Manufacturer · IT , Viadana, Mantova

D.I.R.R.A. S.R.L.

1 submissions · 1 cleared · Since 2004
1
Total
1
Cleared
0
Denied

D.I.R.R.A. S.R.L. — FDA 510(k) Submissions

D.I.R.R.A. S.R.L. has submitted 1 FDA 510(k) premarket notifications since 2004, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include General Surgery Tray . Use the specialty filter in the sidebar to narrow results.

1 devices
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