Medical Device Recalls
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1 result found
510(K) Number: K130209 |
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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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Inspire 6 Integrated Phisio OXY w/ HVR Reservoir, Sterile EO, Catalog # 050713 The intended uses ... | 2 | 05/23/2018 | LivaNova USA |
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