Medical Device Recalls
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1 result found
510(K) Number: K113759 |
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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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AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses | 2 | 01/03/2013 | Cooper Vision Caribbean Corp. |
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