Medical Device Recalls
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1 result found
510(K) Number: K041442 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| EP-4 Computerized Stimulator -- 2 channel and 4 channel. The product consists of a touchscreen port... | 2 | 05/31/2006 | EP Medsystems |
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