L & T S.N.C. DI E. Lucini & C. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
L & T S.N.C. DI E. Lucini & C. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
L & T S.N.C. DI E. Lucini & C. has 1 FDA 510(k) cleared medical devices. Based in Milano, IT.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by L & T S.N.C. DI E. Lucini & C. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - L & T S.N.C. DI E. Lucini & C.
1 devices