Medical Device Recalls
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1 result found
510(K) Number: K161399 |
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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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| Neocis Guidance System Fiducial Array - Product Usage: The Neocis Guidance System (NGS) is a compute... | 2 | 11/21/2019 | Neocis Inc. |
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