Medical Device Recalls
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1 result found
510(K) Number: K033698 |
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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 Straight Ventricular Catheter F8, 25 cm, Sterile EO, Rx only, packaged in a Tyvek pouch and ... | 2 | 09/30/2016 | Integra LifeSciences Corp. |
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