Medical Device Recalls
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1 result found
510(K) Number: K053244 |
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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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Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue Oxygen Monitoring 1) LIC... | 2 | 12/18/2014 | Integra LifeSciences Corp. |
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