Medical Device Recalls
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1 result found
510(K) Number: K053308 |
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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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Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s): N/A Software Version(s): A... | 2 | 03/11/2014 | Horiba Instruments, Inc dba Horiba Medical |
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