Medical Device Recalls
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1 result found
510(K) Number: K051178 |
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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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MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stim... | 2 | 02/17/2016 | Nihon Kohden America Inc |
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