Medical Device Recalls
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1 result found
510(K) Number: K935958 |
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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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| CRIT-LINE Blood Chamber- an accessory to the Crit line III- Monitors in real time blood parameters ... | 2 | 06/05/2015 |
FEI # 3001451489 Fresenius Medical Care Holdings, Inc. |
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