FDA 510(k) Applications Submitted by Mette Andersen
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230332 | 02/07/2023 | Ambu« aScopeÖ Colon; Ambu« aBoxÖ 2 | Ambu A/S |
| K232919 | 09/19/2023 | Ambu« aScopeÖ Gastro Large; Ambu« aBoxÖ 2 | Ambu A/S |
| K233886 | 12/08/2023 | Ambu« aScopeÖ Duodeno 2, Ambu« aBoxÖ 2 | Ambu A/S |
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