Medical Device Recalls
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1 result found
510(K) Number: K082033 |
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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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| Sybaritic, NannoLight MP50. Model Numbers and Description: 1.) 304207-MP 220 Volt, Multi-Pl... | 2 | 09/03/2009 |
FEI # 2131125 Sybaritic, Inc |
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