Resmed Corporation
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-in recall (Z-0746-2016) | Resmed Corporation | 2016-02-03 |
| ResMed S8 Continuous Positive Airway Pressure (CPAP) Flow generator with the following mod recall (Z-1006-2007) | Resmed Corporation | 2007-07-03 |
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Every clearance here is in the API, with alerts when new ones post.