Medical Device Recalls
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1 result found
510(K) Number: K170784 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PNEUMOCLEAR Heated High-Flow Tube Set Product Usage: The Heated High-Flow Tube Set is a single ... | 2 | 11/27/2018 | WOM World of Medicine AG |
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