Medical Device Recalls
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1 result found
510(K) Number: K031522 |
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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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SOLO-care® Plus with Aqualube, Multi-purpose solution*** AquaSoft (Private label), Multi-purpose so... | 2 | 10/21/2004 | Ciba Vision Corporation |
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