Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K140862 |
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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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Uterine Electromyographic Monitor - Monica Novii Wireless Patch System Product Usage: The Novii ... | 2 | 03/14/2018 | GE Healthcare, LLC |
Monica Novii Wireless Patch System product Usage: Novii Interface - The Novii Interface is an ac... | 2 | 05/25/2017 | MONICA HEALTHCARE LTD |
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