Medical Device Recalls
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1 result found
510(K) Number: K172258 |
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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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| Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: ... | 1 | 04/23/2025 |
FEI # 3012198618 Conavi Medical Inc. |
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