Medtronic Cardiac Surgery, Medtronic, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K960755 | CARDIOTHERM BLOOD CARDIOPLEGIA SYSTEMS | DQX | 1996-05-23 | View |
| 510(k) | K953564 | MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE | DTL | 1996-02-02 | View |
No matching devices.
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