Resmed Pty Ltd (Registration Number: 3004604967)
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2024-09-24
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K234134 | AirFit F30i Mask System; AirFit F30i NM Mask System; Arcadia Mask System | BZD | 2024-09-24 | View |
| 510(k) | K230476 | Oran Park Mask | BZD | 2023-10-19 | View |
| 510(k) | K223747 | Whitsundays Mask System | BZD | 2023-07-06 | View |
No matching devices.