Medical Device Recalls
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1 result found
510(K) Number: K924600 |
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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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Integral Lumbar Drainage Set, REF 910420, Sterile EO, Rx only, primary packaged in a PVC blister sea... | 2 | 09/30/2016 | Integra LifeSciences Corp. |
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