Medical Device Recalls
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1 result found
510(K) Number: K051460 |
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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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CardioMD III (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray system... | 2 | 06/11/2015 | Philips Medical Systems (Cleveland) Inc |
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