Medical Device Recalls
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1 result found
510(K) Number: K060705 |
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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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| Carina Home Ventilator. The device is used as a continuous respirator/ventilator for home use. | 2 | 05/14/2009 |
FEI # 2517967 Draeger Medical, Inc. |
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