Ambu A/S · Class II · Cleared Jan 4, 2024
| K-number | K233671 |
| Device name | Ambu® aScope 5 Broncho 4.2/2.2; Ambu® aScope 5 Broncho 2.7/1.2; Ambu® aView 2 Advance |
| Applicant | Ambu A/S |
| Product code | EOQ |
| Device class | Class II |
| Decision date | Jan 4, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 874.4680 |
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