Medical Device Recalls
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1 result found
510(K) Number: K950976 |
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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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| Injection Needle, 3 Fr., REF: 27030N; Injection Cannula, 6 Fr., REF: 27182A | 2 | 12/18/2023 |
FEI # 3007475226 Karl Storz Endoscopy |
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