Medical Device Recalls
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1 result found
510(K) Number: K173713 |
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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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HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.0... | 2 | 08/14/2019 | NeuroLogica Corporation |
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