Medical Device Recalls
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1 result found
510(K) Number: K113703 |
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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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| BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A), Product Order Number Biotrue SVS - 7201, STERILE... | 2 | 11/04/2015 | Bausch & Lomb Inc Irb |
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