FDA 510(k) Applications Submitted by Mingye Zhang
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K233630 | 11/13/2023 | Ambu« aScopeÖ 5 Uretero (Standard Deflection); Ambu« aScopeÖ 5 Uretero (Reverse Deflection); Ambu« aBoxÖ 2 | Ambu A/S |
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