Medical Device Recalls
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1 result found
510(K) Number: K192370 |
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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: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic Syringe Catalog/REF Nu... | 2 | 11/23/2020 |
FEI # 2520313 Bayer Medical Care, Inc. |
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