Medical Device Recalls
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1 result found
510(K) Number: K051262 |
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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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Respironics Esprit Ventilator System, Model Number V1000 with Optional External Battery; Product Num... | 2 | 08/11/2009 | Respironics California Inc |
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