Medical Device Recalls
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1 result found
510(K) Number: K060369 |
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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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Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to be used for calibration of th... | 2 | 01/07/2016 | Siemens Healthcare Diagnostics Inc |
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