Medical Device Recalls
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1 result found
510(K) Number: K103090 |
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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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| Terumo BCT Lakewood, CO 80215, Catalog No 61000 Spectra Optia Apheresis System, Country of Origin: U... | 2 | 05/30/2012 |
FEI # 1000117351 CaridianBCT, Inc. |
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