Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K082142 |
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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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| ACUSON S2000 ultrasound system Manufactured by Siemens Medical Solutions USA, Inc. Business Unit U... | 2 | 04/22/2011 |
FEI # 2936884 Siemens Medical Solutions USA, Inc. |
| Siemens brand ACUSON S2000 Ultrasound System with software versions: VA10, VA10A, VA10B, VA10C, VA1... | 2 | 04/06/2011 |
FEI # 2936884 Siemens Medical Solutions USA, Inc. |
| TEE Transducer V5M, when used with the Acuson S2000 Ultrasound System, software versions: VA15, VA15... | 2 | 04/04/2011 |
FEI # 2936884 Siemens Medical Solutions USA, Inc. |
| ACUSON S2000 ultrasound systems (all versions) with cardiovascular options installed; ACUSON S2000:... | 2 | 03/28/2011 |
FEI # 2936884 Siemens Medical Solutions USA, Inc., Mountain View, CA |
| V5M TEE Transducer, when used with an ACUSON S2000 ultrasound system that has cardiac options instal... | 2 | 02/22/2011 |
FEI # 2936884 Siemens Medical Solutions USA, Inc. |
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