Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K940484 |
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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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| Coroskop X-Ray System, Model numbers 6258219 and 6379759. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Bicor X-Ray System, Model number 9023136. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Bicor Hi-P X-Ray System, Model numbers 6379767 and 6258383. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Coroskop Top X-Ray System, Model number 6134808. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| BICOR TOP X-Ray System, Model number 6134816. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| BICOR HS X-Ray System, Model number 6005776 | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| COROSKOP HS-ACS X-Ray System, Model number 6134659. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| BICOR POLYDOROS X-Ray System, Model number 6134667. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Coroskop C X-Ray System, Model numbers 6005636 and 9108572. | 2 | 11/04/2008 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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