Medical Device Recalls
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1 result found
510(K) Number: K081661 |
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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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3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite; Affiniti 30, 50, and 70; Cle... | 2 | 09/06/2023 | Philips Ultrasound, Inc. |
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