Medical Device Recalls
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1 result found
510(K) Number: K152881 |
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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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Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming... | 2 | 12/10/2020 | Spacelabs Healthcare, Ltd. |
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