Medical Device Recalls
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1 result found
510(K) Number: K142876 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or 6C1 HD biopsy guidelines 6C1HD - ... | 2 | 08/05/2015 | Siemens Medical Solutions USA, Inc. |
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