Medical Device Recalls
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1 result found
510(K) Number: K062284 |
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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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CES Ultra, Cranial Electrotherapy Stimulator, Serial Numbers: 1000 through 3999, Manufactured by Ar... | 2 | 04/08/2008 | Neuro-Fitness LLC |
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