Medical Device Recalls
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1 result found
510(K) Number: K041212 |
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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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HOUVA III Phototherapy System with DermaSense Technology comes on one skid within 10 cardboard boxes... | 3 | 08/28/2008 | National Biological Corp |
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