Medical Device Recalls
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1 result found
510(K) Number: K062892 |
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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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Smiths Medical CADD-Sentry Pro Medication Safety Software - electronic pump protocol programming sof... | 2 | 02/26/2008 | Smiths Medical MD, Inc. |
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