Medical Device Recalls
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1 result found
510(K) Number: K010598 |
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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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Quantimetrix Synovialscopics Synovial Fluid Control. Synovialscopics is a plastic bottle Synovia... | 2 | 01/17/2009 | Quantimetrix Corporation |
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