Pulmonox Medical, 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) | K033779 | VIANOX DELIVERY SYSTEM, MODEL II | MRN | 2004-01-26 | View |
| 510(k) | K023014 | VIANOX DELIVERY SYSTEM, MODEL I | MRP | 2003-08-14 | View |
No matching devices.
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