Medical Device Recalls
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1 result found
510(K) Number: K974814 |
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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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| SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9C... | 2 | 12/09/2021 | Argon Medical Devices, Inc |
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