Medical Device Recalls
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1 result found
510(K) Number: K132547 |
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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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Monarch Medical Technologies EndoTool IV, Versions 1.8, Version 1.8.5 and higher, and Version 1.9 an... | 2 | 06/15/2019 | Monarch Medical Technologies |
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