Medical Device Recalls
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1 result found
510(K) Number: K071234 |
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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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| Siemens Medical Solutions USA, Inc., ACUSON AcuNav ultrasound catheters when using SwiftLink cathet... | 2 | 03/23/2011 |
FEI # 2936884 Siemens Medical Solutions USA, Inc. |
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