Medical Device Recalls
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1 result found
510(K) Number: K161843 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 TUS AI800 diagnostic ultrasound system | 2 | 07/10/2017 |
FEI # 2020563 Toshiba American Medical Systems Inc |
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