Medical Device Recalls
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1 result found
510(K) Number: K970801 |
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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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| BCI Non Invasive Blood Pressure Monitor Product/Catalog number 6004, | 2 | 08/25/2008 |
FEI # 2183502 Smiths Medical PM, Inc. |
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