Medical Device Recalls
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1 result found
510(K) Number: K083538 |
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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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NeuroStar TMS Therapy System/SenStar Treatment Link. The SenStar Treatment Link is a single use, ... | 2 | 05/27/2009 | Neuronetics, Inc. |
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