Medical Device Recalls
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1 result found
510(K) Number: K112881 |
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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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| NBS System 4 (sw version 4.0 or higher), Software update to 4.3.3 and NBS System 5 (sw version 5.0 o... | 2 | 05/22/2017 |
FEI # 3007147067 Nexstim PLC |
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