Medical Device Recalls
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1 result found
510(K) Number: K900519 |
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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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| Reusable, Self-Adhering TENS/NMES/FES electrodes Single Patient Use Only. An electrocardiograph ... | 2 | 12/10/2012 | Covidien LLC dba Uni-Patch |
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