Medical Device Recalls
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1 result found
510(K) Number: K982905 |
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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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| 11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018); 11278AC1 N/A Flexible Ureteroscope Z1... | 2 | 05/12/2022 |
FEI # 3007475226 Karl Storz Endoscopy |
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