Medical Device Recalls
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41 to 42 of 42 Results
510(K) Number: K182809 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System | 2 | 12/08/2019 | Integra LifeSciences Corp. |
C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System | 2 | 12/08/2019 | Integra LifeSciences Corp. |
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