Medical Device Recalls
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1 result found
510(K) Number: K031566 |
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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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| Baxter Healthcare Corporation, Medication Delivery Division, Syndeo PCA Syringe Pump, product codes ... | 2 | 08/16/2005 |
FEI # 1416980 Baxter Healthcare Corp. |
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