Sorin Biomedical, Inc.
Sorin Biomedical, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 1999.
Top product codes for Sorin Biomedical, Inc.
Recent clearances by Sorin Biomedical, Inc.
- K990103 — MONOLYTH C 600 AND 1200 HOLLOW FIBER MEMBRANE LUNG WITH INTEGRATED SOFTSHELL VENOUS RESERVOIR , CVR 600 AND 1200 SOFTSHE
- K963758 — CODE 150 BLOOD COMPONENT COLLECTION SET AND WITH DIRECT DRAW LINE
- K963759 — DIDECO COMPACT-A AND COMPACT-M AUTOTRANSFUSION SYSTEMS
- K964908 — VRF40 VENOUS RESERVOIR WITH INTEGRAL CARDIOTOMY FILTER
- K964907 — VENOMIDICARD PEDIATRIC VENOUS RESERVOIR WITH INTEGRALCARDIOTOMY FILTER/MIDICARD PEDIATRIC CARDIOTOMY RESERVOIR WITH FILT
- K961869 — DIDECO NEWBORN/INFANT ARTERIAL FILTERS: D735 MICRO 20 AND D736 MICRO 40
- K952270 — DIDECO ADULT ARTERIAL FILTERS D732 MICRO 20 W/20, D734 MICRO 40 W/40 MICRON SCREEN
- K945198 — DIDECO PEDIATRIC ARTERIAL FILTERS
- K945065 — DIDECO FLEXIBLE RESERVOIR -- PRODUCT DESIGNATION 5063
- K941215 — VENOMIDICARD INFANT/ PEDIATRIC VENOUS CARDIOTOMY RESERVOIR
- K942582 — SORIN BLOOD CARDIOPLEGIA CONSOLE
- K934763 — SORIN BLOOD CARDIOPLEGIA SYSTEM
- K934847 — NGBCD & NGBCDP CARDIOPLEGIA DELIVERY SYSTEMS
- K936183 — SORIN BCD ADVANCED PEDIATRIC BLOOD CARDIOPLEGIA SYSTEMS
- K933481 — SORIN MONOLYTH VENOUS RESERVOIR
Data sourced from openFDA. This site is unofficial and independent of the FDA.