AirFit N20 — Resmed, Ltd. (510(k) K161978)
AirFit N20 — Resmed, Ltd. (510(k) K161978) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: AirFit N20; Applicant: Resmed, Ltd.; Clearance track: 510(k).
| Device name | AirFit N20 |
|---|---|
| Applicant | Resmed, Ltd. |
| Clearance track | 510(k) |
| Submission number | K161978 |
| Decision | Substantially Equivalent |
| Decision date | 2016-11-17 |
| Date received | 2016-07-18 |
| Product code | BZD |
| Device class | 2 |
| Medical specialty | Anesthesiology |
| Applicant location | AU |
| Source | openFDA device |
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