Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K222648 |
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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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5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/795143, 5500 W/795144, 5... | 2 | 05/03/2024 | Philips Ultrasound, Inc. |
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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