M.D.L. S.R.L. is one of 196 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
M.D.L. S.R.L. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
M.D.L. S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Delebio (So), IT.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by M.D.L. S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vantage Consulting International, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - M.D.L. S.R.L.
1 devices