Medical Device Recalls
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1 result found
510(K) Number: K063490 |
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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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Intesys Clinical Suite (ICS) G2 92810 Smart Disclosure. The Smart Disclosure product collects patie... | 2 | 08/25/2010 | Spacelabs Healthcare, Incorporated |
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