Inogen, 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) | K241091 | SIMEOX 200 Airway Clearance Device | SDT | 2024-12-23 | View |
| 510(k) | K230052 | Inogen Rove 6 | CAW | 2023-06-30 | View |
| 510(k) | K032818 | INOGEN ONE OXYGEN CONCENTRATOR | CAW | 2004-05-13 | View |
No matching devices.
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