Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061515 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Baxter Renal Software Suite v.3.0 and v.3.1 - Renal Link HD Module; clinical data management softwar... | 2 | 01/26/2008 | Baxter Healthcare Renal Div |
| Baxter RenalSoft v.2.0 Patient Management Software Suite - HD Module; clinical data management soft... | 2 | 01/26/2008 | Baxter Healthcare Renal Div |
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