Medical Device Recalls
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1 result found
510(K) Number: K163702 |
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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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Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit ... | 2 | 06/29/2018 | Toshiba American Medical Systems Inc |
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