Medical Device Recalls
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1 result found
510(K) Number: K982594 |
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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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The product is a sheath meant to fit over a Nasopharyngoscope and is labeled as EndoScrub 2 Sheaths | 3 | 07/20/2004 | Medtronic Xomed, Inc. |
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