Medical Device Recalls
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1 result found
510(K) Number: K083523 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Blue Diamond Digital Inflation Device, REF: IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, IN7130... | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
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