Medical Device Recalls
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1 result found
510(K) Number: K901575 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Reusable, non-sterile, self-adhering electrodes for use with TENS/NMES, . Made in the U.S.A. Cutan... | 2 | 12/10/2012 | Covidien LLC dba Uni-Patch |
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