Medical Device Recalls
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1 result found
510(K) Number: K092359 |
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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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EchoTip® Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012 | 2 | 05/16/2024 | Cook Medical Incorporated |
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