Medical Device Recalls
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1 result found
510(K) Number: K182821 |
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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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Accutorr 7 Vital Signs Monitor with NIBP valve assembly board, p/n 115-017679-00, containing softwar... | 2 | 10/29/2019 | Mindray DS USA, Inc. dba Mindray North America |
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