Medical Device Recalls
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1 result found
510(K) Number: K883239 |
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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 CAPD Solution Transfer Set for use with UV-Flash Germicidal Exchange Device, 1.2 m (48''); a ... | 2 | 12/09/2004 |
FEI # 3000210122 Baxter Healthcare Renal Div |
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