Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K041218 |
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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| Philips Medical Systems -- Cardiac Viewer or Pulmonary Viewer software application version 2.0 in us... | 2 | 02/08/2008 |
FEI # 1525965 Phillips Nuclear Medicine |
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