Medical Device Recalls
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1 result found
510(K) Number: K030787 |
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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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Shiley FlexTra brand Flexible Dual-Cannula Tracheostomy Tube, Models: 358060, Size 6, FlexTra Cuf... | 2 | 04/22/2005 | Nellcor Puritan Bennett |
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