Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K103483 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ingenuity TF PET/MRI System v.3.7.1, 510(k) #K103483, Model #882380. The device is a diagnostic ... | 2 | 05/22/2012 | Philips Medical Systems (Cleveland) Inc |
| Ingenuity TF Positron Emission Tomography (PET) and Magnetic Resonance Imaging (MRI), 882380, Philip... | 2 | 05/28/2015 | Philips Medical Systems (Cleveland) Inc |
| Ingenuity PET/MR (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray s... | 2 | 06/11/2015 | Philips Medical Systems (Cleveland) Inc |
| Ingenuity TF PET/MR, Diagnostic Imaging System , Philips Medical Systems | 2 | 08/31/2015 | Philips Medical Systems (Cleveland) Inc |
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