Medical Device Recalls
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1 result found
510(K) Number: K162329 |
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Transducer S7-3t UDI (01)00884838061439 REF 989605406772 Can be used with: CX50, EPIQ 7, Affi... | 2 | 05/01/2020 | Philips Ultrasound Inc |
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