Medical Device Recalls
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1 result found
510(K) Number: K102048 |
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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 Jarit GEMINI CLAMP 9 1/4 inch - used in vascular and cardiothoracic procedures used for clam... | 2 | 08/30/2019 | Integra LifeSciences Corp. |
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