Medical Device Recalls
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1 result found
510(K) Number: K152902 |
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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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TI Transport Monitor/Module Battery Pack Product Usage: intended for monitoring, displaying, rev... | 2 | 06/27/2017 | Mindray DS USA, Inc. dba Mindray North America |
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