Medical Device Recalls
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1 result found
510(K) Number: K103788 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| PENTRA C200, Part Number: A11A01629. The Pentra C200 system is a fully automated chemistry analyz... | 2 | 01/03/2013 | Horiba Instruments, Inc dba Horiba Medical |
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