Medical Device Recalls
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1 result found
510(K) Number: K855058 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Integra Drainage Accessory Kits, REF 910122, Sterile EO, Rx only, packaged in one Tyvek pouch. Five ... | 2 | 09/30/2016 | Integra LifeSciences Corp. |
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