Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K013521 |
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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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Computed Tomography X-Ray Systems, (Brilliance 6, Brilliance 16, MX8000 Dual v. Exp, GEMINI Dual), P... | 2 | 09/25/2012 | Philips Medical Systems (Cleveland) Inc |
Gemini PET/CT sytem, Dual Configuration | 2 | 08/30/2005 | Philips Medical Systems (Cleveland) Inc |
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