Medical Device Recalls
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1 result found
510(K) Number: K083895 |
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Results per Page |
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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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| Codman ISOCOOL Bipolar Forceps-are indicated for cauterizing, coagulating, grasping, and manipulatin... | 2 | 08/07/2019 | Integra LifeSciences Corp. |
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