Medical Device Manufacturer · IT , Viadana, Mantova

D.I.R.R.A. S.R.L. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Total

Cleared

Denied

D.I.R.R.A. S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Viadana, Mantova, IT.

Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by D.I.R.R.A. S.R.L. Filter by specialty or product code using the sidebar.

D.I.R.R.A. S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - D.I.R.R.A. S.R.L.

1 devices

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