Medical Device Recalls
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1 result found
510(K) Number: K101325 |
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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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Bausch + Lomb Stellaris PC Vision Enhancement System, Posterior Fluidics Module (PFM). The system is... | 2 | 12/20/2012 | Bausch & Lomb Inc |
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