FDA 510(k) Applications Submitted by Martina Krautwald
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K250269 | 01/30/2025 | Ambu« aScopeÖ 5 Cysto HD (Standard Deflection); Ambu« aScopeÖ 5 Cysto HD (Reverse Deflection) | Ambu A/S |
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