Medical Device Recalls
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1 result found
510(K) Number: K192804 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c) GS9095SD; ... | 1 | 03/13/2024 | Medos International Sarl |
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