Naltiac Medical, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K961717 | NMI RETROGRADE CARDIOPLEGIA CANNULA-RCCS | DWF | 1996-07-18 | View |
| 510(k) | K961181 | NMI VEIN GRAFT PERFUSION SET | DTL | 1996-06-21 | View |
| 510(k) | K961180 | NMI ANTEGRAD CARDIOPLEGIA CANNULA | DWF | 1996-06-21 | View |
No matching devices.
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