Medical Device Recalls
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1 result found
510(K) Number: K153529 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.0... | 2 | 08/14/2019 | NeuroLogica Corporation |
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