Medical Device Recalls
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1 result found
510(K) Number: K092886 |
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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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Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip).... | 2 | 03/03/2017 | Parker Medical |
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