Medical Device Recalls
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1 result found
510(K) Number: K954987 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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System 1000 family of Hemodialysis Instruments, including the System 1000, TINA, AURORA and AltraTou... | 2 | 11/12/2009 | Baxter Healthcare Renal Div |
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