Medical Device Recalls
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1 result found
510(K) Number: K123144 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care | 2 | 07/16/2015 |
FEI # 3003244771 Breas Medical AB |
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