Medical Device Recalls
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1 result found
510(K) Number: K960817 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Transonic Hemodialysis Monitor, Model HD03 -- Product Usage: The Hemodialysis Monitor is inte... | 2 | 03/18/2015 |
FEI # 1319030 Transonic Systems Inc |
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