Home › Device types › QLN
Extracorporeal System For Carbon Dioxide Removal For The Treatment Of Covid-19
FDA product code QLN · Class N · Unknown
0
Registered devices
40
Adverse events
1
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-12-18 | Alung Technologies Inc | CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a component to the Hemolung for EUA, and the infusion pump may have a delivery inaccurac |
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