Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032063 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PEMView Software used with Naviscan PEM Flex Solo I and PEM Flex Solo II PET Scanner, for nuclear me... | 3 | 10/11/2007 |
FEI # 3005945241 Naviscan PET Systems |
| Naviscan PET Systems, Inc ("Naviscan") PEM Flex Solo II PET Scanner. The PEM Flex Solo II images s... | 2 | 09/11/2008 |
FEI # 3005945241 Naviscan PET Systems |
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