Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032036 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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GEMINI PET/CT System, a diagnostic imaging system for fixed or mobile installations that combines Po... | 2 | 11/02/2015 | Philips Medical Systems (Cleveland) Inc |
Gemini 16 PET/CT sytem, Slice Configuration | 2 | 08/30/2005 | Philips Medical Systems (Cleveland) Inc |
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