Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K042419 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Draeger Fabius GS Premium, Fabius OS, Fabius Tiro, Fabius Tiro D-M Product Usage: used to admi... | 1 | 10/10/2013 | Draeger Medical, Inc. |
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