Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K903660 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dermalight 80 Model Number UVB-080, one unit per box. The Dermalight 80 is a Phototherapy light ... | 3 | 07/19/2013 |
FEI # 1521608 National Biological Corp |
| Dermalight 80 Model Number UVB-083, one unit per box. The Dermalight 80 is a Phototherapy light u... | 3 | 07/19/2013 |
FEI # 1521608 National Biological Corp |
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