Medical Device Manufacturer · US , Waltham , MA

Dideco S.P.A. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 1997

Total

Cleared

Denied

Dideco S.P.A. has 22 FDA 510(k) cleared cardiovascular devices. Based in Waltham, US.

Historical record: 22 cleared submissions from 1997 to 2004.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dideco S.P.A.

22 devices

1-12 of 22

Cleared May 06, 2004

D731 MICRO 20 AND D733 MICRO 40 PEDIATRIC ARTERIAL FILTERS

K041061 · DTM

Cardiovascular · 13d

Cleared Jan 13, 2004

D 903 AVANT ADULT HOLLOW FIBER OXYGENATOR AND D 903 AVANT 2 PH.I.S.I.O. ADULT...

K033323 · DTZ

Cardiovascular · 90d

Cleared Jan 08, 2004

D735 MICRO 20 AND D736 MICRO 40 NEWBORN-INFANT ARTERIAL FILTERS

K033987 · DTM

Cardiovascular · 16d

Cleared Dec 11, 2003

MVR 1200 PC: SORIN MONOLYTH VENOUS RESERVOIR 1200 PC WITH PHOSPHORYLCHOLINE...

K033714 · DTN

Cardiovascular · 15d

Cleared Jul 09, 2003

IDEAL MIMESYS SYSTEM WITH INTEGRATED VENOUS AIR REMOVAL, CENTRIFUGAL BLOOD...

K032040 · KFM

Cardiovascular · 8d

Cleared May 02, 2003

SYNTHESIS MIMESYS ADULT MEMBRANE OXYGENATOR

K031223 · DTZ

Cardiovascular · 14d

Cleared Mar 31, 2003

IDEAL: SYSTEM WITH INTEGRATED VENOUS AIR REMOVAL, CENTRIFUGAL BLOOD PUMP,...

K030154 · KFM

Cardiovascular · 74d

Cleared Nov 04, 2002

DHF 0.2 HEMOCONCENTRATOR: DIDECO NEWBORN-INFANT HEMONCENTRATION

K021732 · KDI

Gastroenterology & Urology · 164d

Cleared Oct 22, 2002

INTEGRATED UNIT: SYNTHESIS: ADULT MEMBRANE OXYGENATOR WITH INTEGRATED...

Anesthesiology · 189d

Cleared Apr 04, 2002

APEX PH.I.S.I.O. ADULT HOLLOW FIBER MEMBRANE OXYGENATOR

K020997 · DTZ

Cardiovascular · 7d

Cleared Feb 26, 2002

D 903 AVANT 2 PH.I.S.I.O. ADULT HOLLOW FIBER OXYGENATOR

K020351 · DTZ

Cardiovascular · 22d

Dideco S.P.A. - FDA 510(k) Cleared Devices

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