Medical Device Recalls
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1 result found
510(K) Number: K932483 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human ski... | 2 | 09/12/2014 |
FEI # 2311923 JK Products & Services, Inc |
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