Medical Device Recalls
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1 result found
510(K) Number: K023251 |
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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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Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 ... | 2 | 08/15/2012 | Maquet Inc. |
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