Medical Device Recalls
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1 result found
510(K) Number: K061923 |
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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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Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 and 3HD012. An in vitro diagnostic mu... | 2 | 02/24/2014 | Siemens Healthcare Diagnostics, Inc. |
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