Medical Device Recalls
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1 result found
510(K) Number: K153023 |
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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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Ablatherm(R) Integrated Imaging, High Intensity Ultrasound System For Prostate Tissue Ablation T... | 2 | 10/26/2017 | Edap Technomed Inc. |
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