Medical Device Recalls
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1 result found
510(K) Number: K160107 |
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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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| DiamondTOUCH Digital Inflation Device, REF: IN9135/A, IN9152/A | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
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