Medical Device Recalls
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1 result found
510(K) Number: K100661 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100) | 2 | 12/18/2025 |
FEI # 3008111228 PATH |
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