Medical Device Recalls
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1 result found
510(K) Number: K110751 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use in the treatment of hy... | 2 | 12/23/2020 | Integra LifeSciences Corp. |
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