Medical Device Recalls
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1 result found
510(K) Number: K080908 |
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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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InnerCool RTx Endovascular System, Model Numbers: 861470 (120V), 861472 (240V). Product Usage: T... | 2 | 01/27/2014 | Philips Healthcare |
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