Avecor Cardiovascular, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K973760 | AFFINITY HOLLOW FIBER OXYGENATOR WITH TRILLIUM BIOPASSIVE SURFACE | DTZ | 1998-02-18 | View |
| 510(k) | K964017 | AFFINITY BLOOD PUMP SYSTEM | DTQ | 1997-08-05 | View |
| 510(k) | K971105 | MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEM | DTN | 1997-07-11 | View |
| 510(k) | K952532 | AFFINITY ARTERIAL BLOOD FILTER | DTM | 1995-10-06 | View |
| 510(k) | K940126 | AVECOR PRE-BYPASS FILTER | KRJ | 1994-06-28 | View |
| 510(k) | K936003 | AFFINITY CVR | DTN | 1994-06-20 | View |
| 510(k) | K935717 | AFFINITY VENOUS RESERVIOR BAG | DTN | 1994-05-10 | View |
| 510(k) | K932252 | AFFINITY HOLLOW FIBER OXYGENATOR | DTZ | 1993-11-19 | View |
| 510(k) | K924529 | SIGNATURE(TM) CUSTOM TUBING PACK | DWF | 1993-06-23 | View |
No matching devices.
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