Medical Device Recalls
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1 result found
510(K) Number: K081570 |
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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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| reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Ligh... | 2 | 04/28/2016 | LED Technologies, LLC |
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