Medical Device Recalls
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1 result found
510(K) Number: K941535 |
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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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Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage: indicated for single ... | 2 | 06/16/2021 | Covidien, LP |
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