Medical Device Recalls
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1 result found
510(K) Number: K140860 |
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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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ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative sof... | 3 | 05/18/2020 | Immersivetouch Inc |
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