Inogen
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2022-12-09
SEC Filings: 1 filings on record. Latest: 8-K (2026-07-01). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222086 | Inogen Rove 4 Portable Oxygen Concentrator | CAW | 2022-12-09 | View |
No matching devices.