Medical Device Recalls
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1 result found
510(K) Number: K872604 |
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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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Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated... | 2 | 03/20/2017 | National Biological Corp |
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