Medical Device Recalls
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1 result found
510(K) Number: K073034 |
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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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| AMT Initial Placement Dilator Set. Used to place gastrostomy devices. | 2 | 06/28/2024 |
FEI # 1526012 Applied Medical Technology Inc |
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