Medical Device Recalls
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1 result found
510(K) Number: K181861 |
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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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Embrace2- Indicated for use as an adjunct to seizure monitoring of adults and children age 6 and up ... | 2 | 10/24/2023 | EMPATICA SRL |
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