Medical Device Manufacturer · US , Waltham , MA

Dideco S.R.L. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1996

Recent clearances: D731 MICRO 20 PH.I.S.I.O PEDIATRIC ARTERIAL FILTER, D733 MICRO 40 PH.I.SI.O PEDIATRIC ARTERIAL FILTER, ECC.O SYSTEM, PERFORMA ADULT HOLLOW FIBER MEMBRANE OXYGENATOR

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.

Dideco S.R.L. is one of 13055 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dideco S.R.L.

6 devices

1-6 of 6

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

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