Respironics Georgia, 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) | K011597 | SMARTMONITOR 2, MODEL 4000 | FLS | 2002-01-11 | View |
| 510(k) | K001708 | PROFOX SOFTWARE, MODEL 920M-41 | DQA | 2001-03-01 | View |
No matching devices.
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