Dideco S.R.L. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dideco S.R.L. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Dideco S.R.L. has 6 FDA 510(k) cleared medical devices. Based in Waltham, US.
Historical record: 6 cleared submissions from 1996 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Dideco S.R.L. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dideco S.R.L.
6 devices
Cleared
Oct 20, 2005
D732 MICRO 27 PH.I.S.I.O. ADULT ARTERIAL FILTER
Cardiovascular
21d
Cleared
May 20, 2005
D731 MICRO 20 PH.I.S.I.O PEDIATRIC ARTERIAL FILTER, D733 MICRO 40 PH.I.SI.O...
Cardiovascular
7d
Cleared
May 05, 2005
ECC.O SYSTEM
Cardiovascular
27d
Cleared
Mar 08, 2005
PERFORMA ADULT HOLLOW FIBER MEMBRANE OXYGENATOR
Cardiovascular
14d
Cleared
Feb 01, 2005
D 905 EOS HOLLOW FIBER OXYGENATOR WITH INTEGRATED HARDSHELL VENOUS/CARDIOTOMY...
Cardiovascular
61d
Cleared
Mar 15, 1996
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
Cardiovascular
212d