Medical Device Recalls
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1 result found
510(K) Number: K161882 |
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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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Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System; Catalogue No: C7000 P... | 2 | 02/23/2018 | Integra LifeSciences Corp. |
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